As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch
Cas:3182-95-4
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inquiryWelcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
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inquiryUnique advantages of L-Phenylglycinol Cas 3182-95-4 Guaranteed purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:White to pale yellow crystalline powder Storage:cool dry place Package:1kg/foil b
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inquiryThe above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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inquiryOur main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
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inquiryL-Phenylglycinol Basic information Product Name: L-Phenylglycinol Synonyms: (S)-(-)-2-amino-3-phenyl-1-propanol (L-phenylalaninol);Benzenepropanol, beta-amino-, (S)-;3-Phenyl-2-amino-1-propanol;β-Aminobenzene-1-propanol;L(-)-2-Amino-3-phenyl
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inquiryDensity: 1.0406 (rough estimate) Melting point: 92-94 ° C (lit.) Boiling point: 273.23 ° C (rough estimate) Specific rotation: -23 º (c=5, EtOH) Flash point: 137.5 ° C Steam pressure: 0.0004mmHg at 25 ° C Solubility in chloroform
Cas:3182-95-4
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inquiryProduct Name: L(-)-2-Amino-3-phenyl-1-propanol Cas#:3182-95-4 MF:C9H13NO MW:151.21 Appearance:White Crystalline Powder Storage:Store in cool and dry place, away from sun light. Package:25KG Application:APIs Transportation:By sea or by air Port:Qingd
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
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inquiryAdvantage : LIDE PHARMACEUTICALS LTD. is a mid-small manufacturing-type enterprise, engaged in pharmaceutical intermediates of R&D, custom-made and production, and also involving trading chemicals for export. We have established the R&
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inquiry1. Product advantages ♦ High purity, all above 98.5%, no impurities after dissolution ♦ We will test each batch to ensure quality ♦ OEM and private brand services designed for free ♦ Various cap colors available ♦ W
Cas:3182-95-4
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inquiryOur Adwantage: 1.We have stock so we can delivery quickly at the very day when receive the payment. 2.Best price, first class service, high successful delivery rate. A discount would be given when you make a large order. 3.High quality gua
Cas:3182-95-4
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inquiry1.No Less 8 years exporting experience. Clients can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specialized
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inquiryOur company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At present
Cas:3182-95-4
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inquiryL-PhenylglycinolCAS:3182-95-4 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic intermedia
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
Appearance:slightly yellow to off- white crystall... Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Used for research and industrial manufacture. Transportation:C
Cas:3182-95-4
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inquiryOur Services 1. New Molecules R&D 2. Own test center HPLC NMR GC LC-MS 3. API and Intermediates from China reputed manufacturers 4. Documents support COA MOA MSDS DMF open part Our advantages 1. Government awarded company. Top 100 enter
Name L-Phenylglycinol Synonyms L(-)-2-Amino-3-phenyl-1-propanol; L-2-amino-3-phenylpropan-1-ol; (S)-2-Amino-3-phenyl-1-propanol; (S)-(-)-2-Amino-3-phenyl-1-propanol; L-(-)-Phenylalaninol
J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
Chemlyte Solutions believe that customers and suppliers deserve much more than what traditional distributors can offer. To grow in today s fast-paced and increasingly competitive market it is essential to be able to quickly adapt to market forces eff
Massive Chemical is certified with ISO9001 and ISO14001 manufacturer for this product. We will offer all documents as requirement for the materials which includes, Certificate of Analysis, Material Safety Data Sheet, and Method of Analysis and
Cas:3182-95-4
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inquiryZibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
Cas:3182-95-4
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inquiryProduct Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
Amino Acid 99% cas 3182-95-4 99% L-Phenylglycinol Powder Pharmaceutical Chemical Pharmaceutical Raw Material MOQ: 1kg Form: Powder Colour: White Test: HPLC Function: amino acid
Cas:3182-95-4
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inquiryGMP standard, high purity, competitive price, in stock 1. Quick Response: within 6 hours after receiving your email. 2. Quality Guarantee: All products are strictly tested by our QC, confirmed by QA, and approved by a third-party lab in China, USA,
High quality, competitive price, fast delivery and first-class service we possesses have won the trust and praise of customers. Standard: BP/USP/EP The purity is equal or greater than 99%. As a supplier, we can provide high-quality products. Cle
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inquiryProduct Name: L-Phenylglycinol Synonyms: ((1S)-1-HydroxyMethyl-2-phenylethyl)aMine;(2S)-2-AMino-3-phenyl-1-propanol;(S)-(-)-2-AMino-3-phenyl-1-glycinol;(S)-2-AMino-1-hydroxy-3-phenylpropane;(βS)-β-AMino-benzenepropanol;(S)-(-)-2-AMINO
Cas:3182-95-4
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryConditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran Heating; | 100% |
With lithium borohydride; chloro-trimethyl-silane In tetrahydrofuran at 0 - 20℃; for 16h; | 99% |
With sodium tetrahydroborate; iodine In tetrahydrofuran at 0℃; for 18.5h; Inert atmosphere; Reflux; | 99% |
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate; diborane In tetrahydrofuran at 20℃; for 1h; | 100% |
With hydrogen In ethanol at 110℃; under 30003 Torr; Reagent/catalyst; Autoclave; chemoselective reaction; | 91.1% |
With lithium aluminium tetrahydride In tetrahydrofuran for 4h; Heating; | 86% |
L-Phenylalaninol
Conditions | Yield |
---|---|
With sodium tetrahydroborate at 23℃; for 2160h; Reduction; | 99% |
Conditions | Yield |
---|---|
With ammonium formate; palladium on activated charcoal In methanol for 0.0833333h; | 98% |
With hydrogen; palladium on activated charcoal In tetrahydrofuran; methanol under 760 Torr; for 3h; Ambient temperature; |
(9-fluorenylmethoxycarbonyl)-L-phenylalaninol
L-Phenylalaninol
Conditions | Yield |
---|---|
With piperidine In dichloromethane for 1h; Ambient temperature; | 85% |
L-Phenylalaninol
Conditions | Yield |
---|---|
With sodium tetrahydroborate at 23℃; for 120h; Reduction; | 85% |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran at 0℃; for 18h; Reflux; | 85% |
(-)-3-[2-(1-hydroxy-3-phenylpropyl)]-4-phenyloxazolidin-2-one
L-Phenylalaninol
Conditions | Yield |
---|---|
With ammonia; lithium at -78℃; for 0.0833333h; | 81% |
(S)-4-Benzyl-2-oxazolidinone
L-Phenylalaninol
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol; water at 100℃; for 72h; | 80% |
Conditions | Yield |
---|---|
With sodium tetrahydroborate In ethanol 1.) room temperature, 4 h, 2.) reflux, 6 h, 3.) room temperature, overnight; | 78% |
With sodium tetrahydroborate In ethanol; water for 18h; Heating; | 74% |
Stage #1: methyl (2S)-2-amino-3-phenylpropanoate hydrochloride With triethylamine In methanol; diethyl ether at -10℃; for 1h; Stage #2: With sodium tetrahydroborate In methanol at 0 - 20℃; | 2.72 g |
Stage #1: methyl (2S)-2-amino-3-phenylpropanoate hydrochloride With sodium tetrahydroborate In water at 0 - 5℃; for 16h; Stage #2: With hydrogenchloride In water pH=5; Stage #3: With sodium hydroxide In water for 3h; Reflux; | 50 g |
(S)-N-tert-butoxycarbonyl-2-amino-3-phenylpropanol
L-Phenylalaninol
Conditions | Yield |
---|---|
With sodium dodecyl-sulfate; benzyl bromide In water at 45 - 50℃; for 48h; chemoselective reaction; | 76% |
With trifluoroacetic acid Substitution; | |
In trifluoroacetic acid for 0.5h; | |
With trifluoroacetic acid In dichloromethane |
Conditions | Yield |
---|---|
With sodium tetrahydroborate In ethanol; water for 4.5h; Reflux; | 72% |
With sodium tetrahydroborate In ethanol for 5.5h; Heating; | 71.7% |
With sodium tetrahydroborate In ethanol | |
With sodium tetrahydroborate In ethanol; water for 4h; Heating; Yield given; | |
With sodium tetrahydroborate In ethanol; water for 4.5h; Reflux; | 19.16 g |
(S)-dibenzyl 1-(1-hydroxy-3-phenylpropan-2-yl)-hydrazine-1,2-dicarboxylate
L-Phenylalaninol
Conditions | Yield |
---|---|
With hydrogen; nickel; acetic acid In methanol at 20℃; under 3102.97 Torr; for 16h; | 70% |
Conditions | Yield |
---|---|
With C24H20ClN2OPRu; potassium tert-butylate; hydrogen In tetrahydrofuran at 110℃; under 2280.15 - 30402 Torr; for 48h; Catalytic behavior; Solvent; Pressure; Temperature; Inert atmosphere; Schlenk technique; Autoclave; | 63% |
(S)-N-(1-hydroxy-3-phenylpropan-2-yl)picolinamide
L-Phenylalaninol
Conditions | Yield |
---|---|
Stage #1: (S)-N-(1-hydroxy-3-phenylpropan-2-yl)picolinamide With hydrogenchloride In water at 20℃; for 0.0833333h; Inert atmosphere; Stage #2: With zinc In water at 20℃; for 16h; Inert atmosphere; | 60% |
(S)-3-phenyl-2-(1H-pyrrol-1-yl)propan-1-ol
L-Phenylalaninol
Conditions | Yield |
---|---|
Stage #1: (S)-3-phenyl-2-(1H-pyrrol-1-yl)propan-1-ol With ozone In methanol at -78℃; for 2.5h; Stage #2: With thiourea In methanol at 0 - 78℃; for 1.5h; Reagent/catalyst; Solvent; Inert atmosphere; | 60% |
L-phenylalanine hydrochloride
L-Phenylalaninol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran at 0℃; for 12h; Reflux; Inert atmosphere; | 46.1% |
Conditions | Yield |
---|---|
With ammonium hydroxide; ammonium acetate; AmDHK78S/N276T In water at 40℃; for 24h; pH=9; Enzymatic reaction; | 41% |
Conditions | Yield |
---|---|
Stage #1: L-phenylalanine With sodium tetrahydroborate; sulfuric acid In tetrahydrofuran; diethyl ether at 0 - 20℃; for 20h; Inert atmosphere; Stage #2: With hydrogenchloride In water at 20℃; for 2h; | A 26% B 36% |
(L)-phenylalanine ethyl ester hydrochloride
A
L-Phenylalaninol
B
(R)-2-amino-3-phenylpropanol
Conditions | Yield |
---|---|
With methanol; Na/SiO2 In tetrahydrofuran at 0 - 25℃; Bouveault-Blanc reduction; Inert atmosphere; optical yield given as %ee; | A 27% B n/a |
rac-phenylalaninol
L-Phenylalaninol
Conditions | Yield |
---|---|
Stage #1: rac-phenylalaninol With O,O'-dibenzoyl-L-tartaric acid In acetone at 25℃; for 6h; Stage #2: With potassium hydroxide In dichloromethane | 24% |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether | |
With lithium aluminium tetrahydride In diethyl ether | |
With lithium aluminium tetrahydride | |
With sodium tetrahydroborate In ethanol; water |
L-Phenylalaninol
Conditions | Yield |
---|---|
(i) aq. NaBH4, (ii) (hydrolysis); Multistep reaction; |
(S)-(-)-2-amino-1-hydroxy-3-phenylpropane ethyl ester hydrochloride
L-Phenylalaninol
Conditions | Yield |
---|---|
With sodium tetrahydroborate In ethanol; water for 4h; Heating; Yield given; |
Conditions | Yield |
---|---|
With α-chymotrypsin chemically modified with monomethoxypolyethylene glycol (α-CT-PEG) Rate constant; enzymatic hydrolysis at pH 8.0 (phosphate buffer), Km value; |
L-phenylalaninol phenylacetate
A
phenylacetic acid
B
L-Phenylalaninol
Conditions | Yield |
---|---|
With α-chymotrypsin chemically modified with monomethoxypolyethylene glycol (α-CT-PEG) Rate constant; enzymatic hydrolysis at pH 8.0 (phosphate buffer), Km value; |
L-Phenylalaninol
Conditions | Yield |
---|---|
With hydrogenchloride In water at 85 - 90℃; for 48h; Yield given; |
L-Phenylalaninol
Conditions | Yield |
---|---|
With hydrogenchloride In water at 85 - 90℃; for 48h; |
methyl (2S)-2-amino-3-phenylpropanoate
A
L-Phenylalaninol
B
(2S)-2-amino-3-cyclohexyl-1-propanol
Conditions | Yield |
---|---|
With hydrogen; Nishimura catalyst <(45.9% Rh/19.9% Pt) oxide> In methanol at 25℃; under 75007.5 Torr; | A 40 % Spectr. B 40 % Spectr. |
di-tert-butyl dicarbonate
L-Phenylalaninol
(S)-N-tert-butoxycarbonyl-2-amino-3-phenylpropanol
Conditions | Yield |
---|---|
In dichloromethane Acylation; | 100% |
In ethanol at 20℃; | 100% |
In water at 30 - 35℃; for 1h; | 100% |
Conditions | Yield |
---|---|
In methanol for 5h; Ambient temperature; | 100% |
L-Phenylalaninol
N-Benzyloxycarbonyl-L-proline
benzyl 2-[(1-benzyl-2-hydroxyethyl)carbamoyl]pyrrolidine-1-carboxylate
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In tetrahydrofuran at 25℃; for 2.5h; | 100% |
Stage #1: N-Benzyloxycarbonyl-L-proline With 4-methyl-morpholine; isobutyl chloroformate In tetrahydrofuran; N,N-dimethyl-formamide at -9 - -5℃; for 0.1h; Stage #2: L-Phenylalaninol In tetrahydrofuran; N,N-dimethyl-formamide at -5 - 20℃; for 20h; Solvent; Temperature; Reagent/catalyst; | 95% |
With 4-methyl-morpholine; chloroformic acid ethyl ester In ethyl acetate at -15 - 20℃; for 15h; Inert atmosphere; Schlenk technique; | 75% |
Stage #1: N-Benzyloxycarbonyl-L-proline With TEA; chloroformic acid ethyl ester In tetrahydrofuran at 0℃; for 0.5h; Stage #2: L-Phenylalaninol In tetrahydrofuran for 20h; |
Conditions | Yield |
---|---|
With potassium carbonate In ethyl acetate at 120 - 130℃; for 3h; | 100% |
With potassium carbonate In ethanol at 130 - 135℃; for 1h; | 88% |
With potassium carbonate at 135 - 140℃; for 2h; | 84% |
phthalic anhydride
L-Phenylalaninol
(-)-(S)-2-(1-benzyl-2-hydroxyethyl)-1H-isoindole-1,3(2H)-dione
Conditions | Yield |
---|---|
With triethylamine In toluene at 145℃; for 41h; | 100% |
With triethylamine In toluene for 3h; Condensation; Heating; | 96% |
at 200℃; for 3h; | 94% |
L-Phenylalaninol
tert-butyldimethylsilyl chloride
(S)-(-)-2-amino-3-phenyl-1-(tert-butyldimethylsilyloxy)propane
Conditions | Yield |
---|---|
With dmap; triethylamine In dichloromethane at 20℃; for 21h; Substitution; | 100% |
With triethylamine In dichloromethane at 20℃; for 24h; Inert atmosphere; Cooling; | 89% |
With dmap; triethylamine In dichloromethane at 20℃; | 88% |
L-Phenylalaninol
benzene-1,3-dicarbonyl dichloride
N1,N3-bis[(S)-1-hydroxy-3-phenylpropan-2-yl]isophthalamide
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 20℃; for 12h; | 100% |
With triethylamine In dichloromethane at 0 - 25℃; for 8h; | 70% |
With triethylamine In dichloromethane at 0 - 20℃; | 53% |
2-methyl-benzyl alcohol
L-Phenylalaninol
2-{[(E)-(S)-1-Hydroxymethyl-2-phenyl-ethylimino]-methyl}-phenol
Conditions | Yield |
---|---|
With sodium sulfate In methanol for 12h; Heating; | 100% |
In ethanol at 20℃; | |
With magnesium sulfate In methanol Heating; | |
In methanol |
L-Phenylalaninol
3-(triisopropylsilyl)propiolic acid
(1S)-3-(triisopropylsilanyl)propynoic acid (1-benzyl-2-hydroxyethyl)amide
Conditions | Yield |
---|---|
With 4-methyl-morpholine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; for 20h; | 100% |
2,2-dimethylmalononitrile
L-Phenylalaninol
(4S,4S')-(-)-2,2'-(1-methylethylidene)bis[4,5-dihydro-4-(phenylmethyl)oxazole]
Conditions | Yield |
---|---|
With zinc trifluoromethanesulfonate In toluene for 48h; Heating; | 100% |
With zinc(II) chloride In chlorobenzene for 24h; Inert atmosphere; Reflux; | 75% |
With zinc(II) chloride In chlorobenzene for 72h; Reflux; | 24% |
L-Phenylalaninol
(2S)-2-cyanopyrrolidine-1-carboxylic acid benzyl ester
(2S)-2-{(4S)-4-benzyl-4,5-dihydro-1,3-oxazol-2-yl}pyrrolidine-1-carboxylic acid benzyl ester
Conditions | Yield |
---|---|
With zinc(II) chloride In chlorobenzene Heating; | 100% |
L-Phenylalaninol
(2-formylphenyl)(diphenyl)phosphine
(S)-2-(2-(diphenylphosphino)benzylideneamino)-3-phenylpropan-1-ol
Conditions | Yield |
---|---|
With sodium sulfate In ethanol Heating; | 100% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 16h; | 100% |
ethyl trifluoroacetate,
L-Phenylalaninol
(S)-2,2,2-trifluoro-N-(1-hydroxy-3-phenylpropan-2-yl)acetamide
Conditions | Yield |
---|---|
In methanol at 20℃; for 2.5h; | 100% |
tert-butyldicarbonate
L-Phenylalaninol
(S)-N-tert-butoxycarbonyl-2-amino-3-phenylpropanol
Conditions | Yield |
---|---|
With sodium hydroxide In dichloromethane; water at 20℃; for 24h; | 100% |
3-[(phenylcarbamoyl)amino]benzoic acid
L-Phenylalaninol
Conditions | Yield |
---|---|
Stage #1: 3-[(phenylcarbamoyl)amino]benzoic acid With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In dichloromethane at 0℃; for 0.5h; Inert atmosphere; Stage #2: L-Phenylalaninol In dichloromethane at 0 - 20℃; for 16h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With benzotriazol-1-ol; dicyclohexyl-carbodiimide In tetrahydrofuran at 20℃; Inert atmosphere; Cooling with ice; | 100% |
Conditions | Yield |
---|---|
In toluene Reflux; Dean-Stark; stereoselective reaction; | 99.8% |
Dimethyl oxalate
L-Phenylalaninol
(S)-N,N'-bis<1-(hydroxymethyl)-2-phenylethyl>ethanediamide
Conditions | Yield |
---|---|
In methanol at 20℃; for 0.583333h; | 99% |
In methanol at 20℃; for 0.5h; | 99% |
In methanol at 20℃; for 0.0833333h; | 99% |
carbon disulfide
L-Phenylalaninol
(4S)-4-benzyl-1,3-oxazolidine-2-thione
Conditions | Yield |
---|---|
With dihydrogen peroxide; potassium carbonate In ethanol at 50℃; | 99% |
With 2-chloro-1,3-dimethylimidazolinium chloride; triethylamine In dichloromethane at 20℃; for 20h; Condensation; Cyclization; | 98% |
With dihydrogen peroxide; potassium carbonate In ethanol at 50℃; for 0.0833333h; | 98% |
L-Phenylalaninol
1-chloro-2(S)-amino-phenylpropane hydrochloride
Conditions | Yield |
---|---|
With thionyl chloride In N,N-dimethyl-formamide at 120℃; for 2h; | 99% |
With hydrogenchloride; thionyl chloride |
L-Phenylalaninol
methyl chloroformate
N-[(1S)-2-Hydroxy-1-benzylethyl]methoxy carboxamide
Conditions | Yield |
---|---|
With potassium carbonate In methanol at 20℃; Acylation; | 99% |
With potassium carbonate In tetrahydrofuran; water at 0 - 20℃; for 2.16667h; Yield given; |
L-Phenylalaninol
benzyl bromide
(S)-2-(dibenzylamino)-3-phenylpropan-1-ol
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 0℃; for 0.333333h; | 99% |
With potassium carbonate In ethanol; water for 0.5h; Reflux; | 96% |
Stage #1: L-Phenylalaninol With potassium carbonate In methanol; water for 0.166667h; Reflux; Stage #2: benzyl bromide In methanol; water for 1h; Heating; | 93% |
(E)-3-phenylpropenal
L-Phenylalaninol
(S,2E)-2-((E)-3-phenylallylideneamino)-3-phenylpropan-1-ol
Conditions | Yield |
---|---|
In diethyl ether for 1.33333h; Ambient temperature; | 99% |
With magnesium sulfate In dichloromethane at 20℃; for 0.333333h; | 99% |
L-Phenylalaninol
2-methyl-4-methoxy-2H-1,2-benzothiazine-3-carboxylic acid 1,1-dioxide
N-(2-methyl-4-methoxy-2H-1,2-benzothiazine-3-carbonyl)-L-phenylalaninol 1,1-dioxide
Conditions | Yield |
---|---|
With 4-methyl-morpholine; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; benzotriazol-1-ol | 99% |
PVS
L-Phenylalaninol
(S)-3-phenyl-2-((2-(phenylsulfonyl)ethyl)amino)propan-1-ol
Conditions | Yield |
---|---|
In isopropyl alcohol for 48h; Heating; | 99% |
L-Phenylalaninol
ortho-toluoyl chloride
(2S)-2-o-toluamide-3-phenylpropanol
Conditions | Yield |
---|---|
With potassium hydroxide In dichloromethane at 0 - 20℃; | 99% |
With triethylamine In tetrahydrofuran for 1h; |
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