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Cas:138890-62-7
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inquiryhebei yanxi chemical co., LTD who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do research and developm
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inquiryUnique advantages for Brinzolamide Cas 138890-62-7 Guaranteed purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:White to yellow crystalline powder Storage:Cool dry place Package
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inquiryBrinzolamide[CAS:138890-62-7] Name Brinzolamide Synonyms (R)-4-(Ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide Molecular Structure
high quality Appearance:White or off-white Solid Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:shanghai
The 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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Cas:138890-62-7
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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
High purity CAS 138890-62-7 Brinzolamide in stock Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED intermediates (Fluorene,Ca
Cas:138890-62-7
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inquiryOur advantages: 1. All inquiries will be replied within 12 hours. 2. Dedication to quality, supply & service. 3. Strictly on selecting raw materials. 4. Reasonable & competitive price, fast lead time. 5. Sample is available for your eva
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inquiryChemical Name ethambutol dihydrochloride Synonyms 2,2'-(Ethane-1,2-diylbis(azanediyl))bis(butan-1-ol) dihydrochloride;(S,S)-N,N'-Bis(1-hydroxy-2-butyl)ethylenediamine Dihydrochloride;(2S,2
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Cas:138890-62-7
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inquiryBrinzolamideCAS: 138890-62-7 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 intermediat
Cas:138890-62-7
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Product Detail Minimum Order Qty. 10 Gram
Cas:138890-62-7
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Cas:138890-62-7
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inquiryBrinzolamide CAS: 138890-62-7 Specification Items Specification Result Assay 98%-102% 99.58% Appearance White to yellow crystalline po
Henan 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
Product Name: Brinzolamide Synonyms: H-Thieno[3,2-e]-1,2-thiazine-6-sulfonamide, 4-(ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-, 1,1-dioxide, (4R)-;Brinzolamide(R)-4-(Ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazine-6-s
Cas:138890-62-7
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inquiryAppearance:white or light yellow crystalline powder 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:By
Hebei Mojin Biotechnology Co., Ltd,Our business covers more than 30 countries, most of the big customers come from Europe, America and other countries in the world, we can guarantee the quality and price. In recent decades, with the efforts of all em
Cas:138890-62-7
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inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
Cas:138890-62-7
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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
brinzolamide
Conditions | Yield |
---|---|
With sodium thiomethoxide In methanol at 0 - 25℃; for 12h; Reagent/catalyst; | 83% |
brinzolamide
Conditions | Yield |
---|---|
With sodium tetradecyl mercaptan In methanol at 0 - 25℃; Reagent/catalyst; | 81% |
Conditions | Yield |
---|---|
In tetrahydrofuran; water at 0 - 30℃; | 66.3% |
brinzolamide
Conditions | Yield |
---|---|
Stage #1: (R)-3,4-dihydro-4-ethylamino-6-chloro-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazine-1,1-dioxide hydrochloride With sodium hydrogencarbonate Stage #2: With n-butyllithium In tetrahydrofuran; hexane at -40℃; for 1h; | 63% |
Conditions | Yield |
---|---|
In water at 11 - 20℃; for 15h; enantioselective reaction; | 61% |
Stage #1: C20H26N2O9S4; ethylamine In water at 10 - 12℃; for 15h; Stage #2: With hydrogenchloride In water at 20℃; for 1h; Temperature; | 2.4 g |
(R)-3,4-Dihydro-4-hydroxy-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide
ethylamine
brinzolamide
Conditions | Yield |
---|---|
Stage #1: (R)-3,4-Dihydro-4-hydroxy-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide With zinc(II) tosylate; triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 20 - 80℃; for 8h; Stage #2: ethylamine In tetrahydrofuran at 0 - 20℃; for 36h; Product distribution / selectivity; | 49% |
Stage #1: (R)-3,4-Dihydro-4-hydroxy-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide With zinc(II) tosylate; triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 20 - 80℃; Stage #2: ethylamine In tetrahydrofuran at 0 - 20℃; |
(S)-3,4-dihydro-4-hydroxy-2(3-methoxypropyl)-4H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-1,1-dioxide
ethylamine
brinzolamide
Conditions | Yield |
---|---|
Stage #1: (S)-3,4-dihydro-4-hydroxy-2(3-methoxypropyl)-4H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-1,1-dioxide With toluene-4-sulfonic acid; triethylamine In tetrahydrofuran at 0 - 20℃; for 18h; Stage #2: ethylamine In tetrahydrofuran at 0 - 20℃; for 36h; | |
Stage #1: (S)-3,4-dihydro-4-hydroxy-2(3-methoxypropyl)-4H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-1,1-dioxide With triethylamine; p-toluenesulfonyl chloride In tetrahydrofuran at 0 - 20℃; for 18h; Stage #2: ethylamine In tetrahydrofuran at 0 - 20℃; |
brinzolamide
Conditions | Yield |
---|---|
With sodium acetate; hydroxylamine-O-sulfonic acid In hexane at 0 - 20℃; Product distribution / selectivity; |
(R)-3,4-dihydro-4-(N-ethylamino)-2-(3-methoxy)propyl-2H-thieno[3,2-e]-1,2-thiazine-1,1-dioxide
brinzolamide
Conditions | Yield |
---|---|
Stage #1: (R)-3,4-dihydro-4-(N-ethylamino)-2-(3-methoxy)propyl-2H-thieno[3,2-e]-1,2-thiazine-1,1-dioxide With n-butyllithium In tetrahydrofuran; hexane at -60℃; for 8.75h; Inert atmosphere; Stage #2: With sulfur dioxide In tetrahydrofuran; hexane at -65 - 20℃; Stage #3: With sodium acetate trihydrate; hydroxylamine-O-sulfonic acid In ethyl acetate at 0 - 20℃; |
brinzolamide
Conditions | Yield |
---|---|
With chiral-prep-HPLC (Chiralpak IA0.46x15 cm, 5 umChiral-A (IA)002IA00CD-LF007) Resolution of racemate; |
(S)-3,4-dihydro-6-chloro-4-hydroxy-2-(3-methoxypropyl)-4H-thieno[3,2-e]-1,2-thiazine 1,1-dioxide
brinzolamide
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: triethylamine / tetrahydrofuran / 0 - 20 °C 2.1: water; tetrahydrofuran / 0 - 20 °C 2.2: pH 1 - 3 3.1: sodium hydrogencarbonate 3.2: 1 h / -40 °C View Scheme | |
Multi-step reaction with 4 steps 1.1: n-butyllithium / hexane; tetrahydrofuran / 3.5 h / -70 - -66 °C / Inert atmosphere 1.2: 20 °C / pH 4 1.3: 15 h / 0 - 25 °C 2.1: acetonitrile / 19 h / 30 - 85 °C / Reflux 3.1: triethylamine / tetrahydrofuran / 2 h / -10 - -2 °C / Inert atmosphere 4.1: water / 15 h / 11 - 20 °C View Scheme |
brinzolamide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: water; tetrahydrofuran / 0 - 20 °C 1.2: pH 1 - 3 2.1: sodium hydrogencarbonate 2.2: 1 h / -40 °C View Scheme |
(R)-(+)-4-ethylamino-2-(3-methoxypropyl)-3,4-dihydro-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-1,1-dioxide maleate
brinzolamide
Conditions | Yield |
---|---|
With triethylamine In water at 25 - 30℃; for 2h; pH=7 - 8.5; | 45 g |
Brinzolamide hydrochloride
brinzolamide
Conditions | Yield |
---|---|
With triethylamine In water at 25 - 30℃; for 2h; pH=7 - 8.5; | 500 g |
brinzolamide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: triethylamine / tetrahydrofuran / 2 h / -10 - -2 °C / Inert atmosphere 2: water / 15 h / 11 - 20 °C View Scheme | |
Multi-step reaction with 2 steps 1: triphenylphosphine; di-isopropyl azodicarboxylate / dichloromethane / 15 h / 0 - 20 °C / Inert atmosphere 2: sodium thiomethoxide / methanol / 12 h / 0 - 25 °C View Scheme |
brinzolamide
Conditions | Yield |
---|---|
Multi-step reaction with 8 steps 1.1: sodium tungstate (VI) dihydrate; dihydrogen peroxide / water / 19 h / 15 - 35 °C 2.1: pyridinium hydrobromide perbromide; sulfuric acid / ethyl acetate / 1.5 h / 1 - 5 °C / Large scale 3.1: B-chlorodiisopinocampheylborane / tert-butyl methyl ether / 3.5 h / -40 - -32 °C / Inert atmosphere 3.2: 2 h / 0 - 22 °C 4.1: potassium carbonate / dimethyl sulfoxide 5.1: n-butyllithium / hexane; tetrahydrofuran / 3.5 h / -70 - -66 °C / Inert atmosphere 5.2: 20 °C / pH 4 5.3: 15 h / 0 - 25 °C 6.1: acetonitrile / 19 h / 30 - 85 °C / Reflux 7.1: triethylamine / tetrahydrofuran / 2 h / -10 - -2 °C / Inert atmosphere 8.1: water / 15 h / 11 - 20 °C View Scheme |
brinzolamide
Conditions | Yield |
---|---|
Multi-step reaction with 7 steps 1.1: pyridinium hydrobromide perbromide; sulfuric acid / ethyl acetate / 1.5 h / 1 - 5 °C / Large scale 2.1: B-chlorodiisopinocampheylborane / tert-butyl methyl ether / 3.5 h / -40 - -32 °C / Inert atmosphere 2.2: 2 h / 0 - 22 °C 3.1: potassium carbonate / dimethyl sulfoxide 4.1: n-butyllithium / hexane; tetrahydrofuran / 3.5 h / -70 - -66 °C / Inert atmosphere 4.2: 20 °C / pH 4 4.3: 15 h / 0 - 25 °C 5.1: acetonitrile / 19 h / 30 - 85 °C / Reflux 6.1: triethylamine / tetrahydrofuran / 2 h / -10 - -2 °C / Inert atmosphere 7.1: water / 15 h / 11 - 20 °C View Scheme |
brinzolamide
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1.1: B-chlorodiisopinocampheylborane / tert-butyl methyl ether / 3.5 h / -40 - -32 °C / Inert atmosphere 1.2: 2 h / 0 - 22 °C 2.1: potassium carbonate / dimethyl sulfoxide 3.1: n-butyllithium / hexane; tetrahydrofuran / 3.5 h / -70 - -66 °C / Inert atmosphere 3.2: 20 °C / pH 4 3.3: 15 h / 0 - 25 °C 4.1: acetonitrile / 19 h / 30 - 85 °C / Reflux 5.1: triethylamine / tetrahydrofuran / 2 h / -10 - -2 °C / Inert atmosphere 6.1: water / 15 h / 11 - 20 °C View Scheme |
3-acetyl-2,5-dichlorothiophene
brinzolamide
Conditions | Yield |
---|---|
Multi-step reaction with 11 steps 1.1: thiourea / ethanol; water / 2 h / Reflux; Large scale 1.2: 3 h / Reflux; Large scale 2.1: chlorine / toluene / 0.42 h / 8 °C / Cooling with ice 3.1: ammonia / 1 h / 5 - 15 °C 4.1: sodium tungstate (VI) dihydrate; dihydrogen peroxide / water / 19 h / 15 - 35 °C 5.1: pyridinium hydrobromide perbromide; sulfuric acid / ethyl acetate / 1.5 h / 1 - 5 °C / Large scale 6.1: B-chlorodiisopinocampheylborane / tert-butyl methyl ether / 3.5 h / -40 - -32 °C / Inert atmosphere 6.2: 2 h / 0 - 22 °C 7.1: potassium carbonate / dimethyl sulfoxide 8.1: n-butyllithium / hexane; tetrahydrofuran / 3.5 h / -70 - -66 °C / Inert atmosphere 8.2: 20 °C / pH 4 8.3: 15 h / 0 - 25 °C 9.1: acetonitrile / 19 h / 30 - 85 °C / Reflux 10.1: triethylamine / tetrahydrofuran / 2 h / -10 - -2 °C / Inert atmosphere 11.1: water / 15 h / 11 - 20 °C View Scheme |
brinzolamide
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: potassium carbonate / dimethyl sulfoxide 2.1: n-butyllithium / hexane; tetrahydrofuran / 3.5 h / -70 - -66 °C / Inert atmosphere 2.2: 20 °C / pH 4 2.3: 15 h / 0 - 25 °C 3.1: acetonitrile / 19 h / 30 - 85 °C / Reflux 4.1: triethylamine / tetrahydrofuran / 2 h / -10 - -2 °C / Inert atmosphere 5.1: water / 15 h / 11 - 20 °C View Scheme |
3-Acetyl-2-(phenylmethyl)thio-5-chlorothiophene
brinzolamide
Conditions | Yield |
---|---|
Multi-step reaction with 10 steps 1.1: chlorine / toluene / 0.42 h / 8 °C / Cooling with ice 2.1: ammonia / 1 h / 5 - 15 °C 3.1: sodium tungstate (VI) dihydrate; dihydrogen peroxide / water / 19 h / 15 - 35 °C 4.1: pyridinium hydrobromide perbromide; sulfuric acid / ethyl acetate / 1.5 h / 1 - 5 °C / Large scale 5.1: B-chlorodiisopinocampheylborane / tert-butyl methyl ether / 3.5 h / -40 - -32 °C / Inert atmosphere 5.2: 2 h / 0 - 22 °C 6.1: potassium carbonate / dimethyl sulfoxide 7.1: n-butyllithium / hexane; tetrahydrofuran / 3.5 h / -70 - -66 °C / Inert atmosphere 7.2: 20 °C / pH 4 7.3: 15 h / 0 - 25 °C 8.1: acetonitrile / 19 h / 30 - 85 °C / Reflux 9.1: triethylamine / tetrahydrofuran / 2 h / -10 - -2 °C / Inert atmosphere 10.1: water / 15 h / 11 - 20 °C View Scheme |
(S)-3,4-dihydro-4-hydroxy-2(3-methoxypropyl)-4H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-1,1-dioxide
brinzolamide
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: acetonitrile / 19 h / 30 - 85 °C / Reflux 2: triethylamine / tetrahydrofuran / 2 h / -10 - -2 °C / Inert atmosphere 3: water / 15 h / 11 - 20 °C View Scheme | |
Multi-step reaction with 3 steps 1.1: triethylamine / acetonitrile / 5 h / 78 °C 2.1: triethylamine / tetrahydrofuran / 3 h / -10 - -4 °C 3.1: water / 15 h / 10 - 12 °C 3.2: 1 h / 20 °C View Scheme | |
Multi-step reaction with 3 steps 1: acetonitrile / 1 h / 5 - 15 °C / Inert atmosphere 2: triphenylphosphine; di-isopropyl azodicarboxylate / ethyl acetate / 15 h / 0 - 20 °C / Inert atmosphere 3: sodium tetradecyl mercaptan / methanol / 0 - 25 °C View Scheme | |
Multi-step reaction with 3 steps 1: acetonitrile / 1 h / 5 - 15 °C / Inert atmosphere 2: triphenylphosphine; di-isopropyl azodicarboxylate / dichloromethane / 15 h / 0 - 20 °C / Inert atmosphere 3: sodium thiomethoxide / methanol / 12 h / 0 - 25 °C View Scheme |
brinzolamide
Conditions | Yield |
---|---|
Multi-step reaction with 9 steps 1.1: ammonia / 1 h / 5 - 15 °C 2.1: sodium tungstate (VI) dihydrate; dihydrogen peroxide / water / 19 h / 15 - 35 °C 3.1: pyridinium hydrobromide perbromide; sulfuric acid / ethyl acetate / 1.5 h / 1 - 5 °C / Large scale 4.1: B-chlorodiisopinocampheylborane / tert-butyl methyl ether / 3.5 h / -40 - -32 °C / Inert atmosphere 4.2: 2 h / 0 - 22 °C 5.1: potassium carbonate / dimethyl sulfoxide 6.1: n-butyllithium / hexane; tetrahydrofuran / 3.5 h / -70 - -66 °C / Inert atmosphere 6.2: 20 °C / pH 4 6.3: 15 h / 0 - 25 °C 7.1: acetonitrile / 19 h / 30 - 85 °C / Reflux 8.1: triethylamine / tetrahydrofuran / 2 h / -10 - -2 °C / Inert atmosphere 9.1: water / 15 h / 11 - 20 °C View Scheme |
Conditions | Yield |
---|---|
With AmyCoat [tris(3,5-dimethylphenylcarbamate)amylose] (150 x 46 mm id) chiral column In hexane; isopropyl alcohol at 25℃; Reagent/catalyst; Resolution of racemate; |
(S)-2-[(1,1-dimethylethyl)diphenylsilyl]oxypropanoic acid
brinzolamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; Inert atmosphere; | 76% |
brinzolamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; Inert atmosphere; | 76% |
brinzolamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; Inert atmosphere; | 75% |
(2S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-{[(2S)-2-[(tert butyldiphenylsilyl)oxy]propanoyl]oxy}propanoyl]oxy}propanoyl]oxy}propanoyl]oxy}propanoyl]oxy}propanoyl]oxy}propanoyl]oxy}propanoyl]oxy}propanoyl]oxy}propanoyl]oxy}propanoyl]oxy}propanoic acid
brinzolamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; Inert atmosphere; | 74% |
brinzolamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; Inert atmosphere; | 68.6% |
brinzolamide
(R)-4-(ethylamino)-2-(3-hydroxypropyl)-3,4-dihydro-2H-thieno[3,2-e][1,2]thiazine-6-sulfonamide1,1-dioxide
Conditions | Yield |
---|---|
With boron tribromide In dichloromethane at -78 - 25℃; for 24.1667h; Inert atmosphere; | 66% |
Stage #1: brinzolamide With boron tribromide In dichloromethane at -78 - 20℃; for 24.16h; Stage #2: With hydrogenchloride In water; dimethyl sulfoxide | 66% |
brinzolamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; Inert atmosphere; | 65% |
brinzolamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; Inert atmosphere; | 65% |
brinzolamide
(3Z)-3-[(4-{[2-(diethylamino)ethyl]carbamoyl}-3,5-dimethyl-1H-pyrrol-2yl)methylidene]-2-oxo-2,3-dihydro-1H-indol-5-yl (2S)-1-{[(2S)-1-{[(2S)-1-[(1S)-1-({[(4R)-4-(ethylamino)-2-(3-methoxypropyl)-1,1-dioxo-2H,3H,4H-1λ6-thieno[3,2-e][1,2]thiazin-6-yl]sulfonyl}carbamoyl)ethoxy]-1-oxopropan-2-yl]oxy}-1-oxopropan-2-yl]oxy}-1-oxopropan-2-yl butanedioate
Conditions | Yield |
---|---|
With dmap; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 2h; Inert atmosphere; | 46% |
brinzolamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; Inert atmosphere; | 44.3% |
brinzolamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; Inert atmosphere; | 37% |
brinzolamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; Inert atmosphere; | 35% |
brinzolamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; Inert atmosphere; | 32% |
brinzolamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; Inert atmosphere; | 27.3% |
brinzolamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; Inert atmosphere; | 27% |
brinzolamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; Inert atmosphere; | 26% |
brinzolamide
(3Z)-3-[(4-{[2-(diethylamino)ethyl]carbamoyl}-3,5-dimethyl-1H-pyrrol-2yl)methylidene]-2-oxo-2,3-dihydro-1H-indol-5-yl (2S)-1-{[(2S)-1-[(1S)-1-({[(4R)-4-(ethylamino)-2-(3-methoxypropyl)-1,1-dioxo-2H,3H,4H-1λ6-thieno[3,2-e][1,2]thiazin-6-yl]sulfonyl}carbamoyl)ethoxy]-1-oxopropan-2-yl]oxy}-1-oxopropan-2-yl butanedioate
Conditions | Yield |
---|---|
With dmap; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 2h; Inert atmosphere; | 26% |
brinzolamide
(2S)-1-{[(2S)-1-{[(2S)-1-{[(2S)-1{[(2S)-1-{[(2S)-1{[(2S)-1-[(1S)-1-({[(4R)-4-(ethylamino)-2-(3-methoxypropyl)-1,1-dioxo-2H,3H,4H-1λ6-thieno[3,2-c][1,2]thiazin-6-yl]sulfonyl}carbamoyl)ethoxy]-1-oxopropan-2-yl]oxy}-1-oxopropan-2-yl]oxy}-1-oxopropan-2-yl]oxy}-1-oxopropan-2-yl]oxy}-1-oxopropan-2-yl]oxy}-1-oxopropan-2-yl]oxy}-1-oxopropan-2-yl octadecanoate
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; Inert atmosphere; | 25% |
brinzolamide
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; Inert atmosphere; | 24% |
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; | 19.4% |
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 30℃; for 1h; Inert atmosphere; | 8% |
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