Dayangchem's 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. DayangChem can provide different quantities
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inquiryHigh quality 5'-O-Dimethoxytrityl-deoxythymidine CAS 40615-39-2 with factory price Company profile Wuhan Fortuna Chemical Co.,Ltd established in 2006, is a big integrative chemical enterprise being engaged in Pharmaceutical & its interme
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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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inquiry1. Factory price and high quality must be guaranteed, base on 8 years of production and R&D experience2. Free samples will be provided,ensure specifications and quality are right for customer3. Customers will receive the most professional technical s
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inquiryTIANFUCHEM--40615-39-2--5'-O-Dimethoxytrityl-deoxythymidine in stock Our company was built in 2009 with an ISO certificate.In the past 10 years, we have grown up as a famous fine chemicals supplier in China And we had established stabl
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inquiryAbout Product Technical Details 5'-O-Dimethoxytrityl-deoxythymidine Chemical Properties Melting point
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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
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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
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NewCan Biotech Limited was established in 2021 and is primarily engaged in the research, development, production, and sales of sugars, nucleosides, nucleotides, phosphorylated monomers, as well as next-generation antiviral and antitumor drug intermed
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inquiryJ&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
A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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inquirySAGECHEM is a chemical R&D, manufacturing and distribution company in China since 2009, including pharmaceutical intermediates, agrochemical, dyestuff intermediates, organosilicone, API and etc. We also offer a full range of services in custom synthe
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4,4'-dimethoxytrityl chloride
thymidine
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With pyridine; dmap at 20℃; for 5h; | 97% |
With pyridine; dmap at 20℃; for 24h; | 96% |
With pyridine at 20℃; for 12h; | 96% |
2-Azidomethyl-benzoic acid (2R,3S,5R)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With diphenyl(methyl)phosphine In 1,4-dioxane; water at 20℃; for 0.25h; Product distribution; Further Variations:; Catalysts; Reaction partners; Reagents; Solvents; reaction times; | 96% |
thymidine
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With 2,6-di-tert-butyl-4-methylpyridine In nitromethane at 20℃; for 17h; or pyridine, other solvents; | 93% |
With lithium carbonate; N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; Heating; | 74% |
4,4'-dimethoxytrityl chloride
thymidine
A
5'-O-(4-4'-dimethoxytrityl)thymidine
B
3'-O-(4,4'-dimethoxytriphenylmethyl)-5'-O-fluorenylmethoxycarbonylthymidine
Conditions | Yield |
---|---|
With pyridine at 20℃; for 1.5h; | A 93% B n/a |
With pyridine at 20℃; for 1.5h; | A 93% B n/a |
With pyridine at 20℃; for 1.5h; | A 93% B n/a |
pyridine
4,4'-dimethoxytrityl chloride
thymidine
A
benzoic acid 5-(4-benzoylamino-5-methyl-2-oxo-2H-pyrimidin-1-yl)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-yl ester
B
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
at 20℃; for 1.5h; | A n/a B 93% |
4,4'-dimethoxytrityl chloride
A
5'-O-(4-4'-dimethoxytrityl)thymidine
B
3'-O-(4,4'-dimethoxytriphenylmethyl)-5'-O-fluorenylmethoxycarbonylthymidine
Conditions | Yield |
---|---|
With pyridine at 20℃; for 0.5h; | A 93% B n/a |
With pyridine at 20℃; for 1.5h; | A 93% B n/a |
1-((2R,4S,5R)-5-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-{[(E)-2-(3-hydroxy-naphthalen-2-yl)-vinyl]-diisopropyl-silanyloxy}-tetrahydro-furan-2-yl)-5-methyl-1H-pyrimidine-2,4-dione
A
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
In methanol for 0.75h; Irradiation; | A n/a B 92% |
In methanol for 0.75h; Irradiation; | A 92% B 91% |
triethylammonium 5'-O-dimethoxytritylthymidine 3'-H-phosphonate
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With pivaloyl chloride; ethylene glycol at 0℃; for 0.333333h; Hydrolysis; | 91% |
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With tri-n-butyl-tin hydride In toluene at 115℃; for 0.0833333h; | 82% |
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In tetrahydrofuran; water for 3h; Ambient temperature; | 73% |
4,4'-dimethoxytrityl alcohol
thymidine
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With ambelyst-15 In dichloromethane for 4h; Reflux; Molecular sieve; regioselective reaction; | 70% |
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0 - 20℃; for 2h; Inert atmosphere; Schlenk technique; | 61% |
2,2'-anhydro-1-[2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-β-D-arabinofuranosyl-5-methyluridine]
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With 15-crown-5; sodium bis(2-methoxyethoxy)aluminium dihydride In 1,2-dimethoxyethane; toluene at 0 - 20℃; for 21h; Product distribution / selectivity; | 35% |
Stage #1: 2,2'-anhydro-1-[2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-β-D-arabinofuranosyl-5-methyluridine] With sodium bis(2-methoxyethoxy)aluminium dihydride In toluene at 0 - 5℃; for 2.91667h; Stage #2: With water at 5℃; for 0.5h; Product distribution / selectivity; | 21% |
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; water at 20℃; Product distribution; |
3'-O-(4,4'-dimethoxytrityl)thymidin-5'-yl 5'-O-(4,4'-dimethoxytrityl)thymidin-3'-yl ethyl phosphonate
A
3'-O-(4,4'-dimethoxytrityl)thymidine
B
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With ethanolamine In pyridine for 0.25h; |
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; water at 20℃; for 23h; Product distribution; |
ethanolamine
5'-O-(4,4'-dimethoxytrityl)thymidin-3'-yl ethyl phosphonate
A
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
In pyridine |
5'-O-(4,4'-dimethoxytrityl)thymidin-3'-yl ethyl phosphonate
A
5'-O-(4-4'-dimethoxytrityl)thymidine
B
phosphonic acid diethyl ester
Conditions | Yield |
---|---|
With ethanol In pyridine for 96h; Yield given. Yields of byproduct given; |
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; water at 20℃; Product distribution; |
C49H52ClN4O17P2(1-)
A
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; water at 20℃; Product distribution; |
5′-O-(4,4′-dimethoxytrityl)thymidine-3′-O-[2-cyanoethyl]phosphonate
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With 1H-imidazole In methanol for 72h; Ambient temperature; Yield given; |
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In tetrahydrofuran for 8h; Product distribution; other bases (piperidine, TBAF, conc. aq. NH3); mechanism of cleavage of succinyl-anchored nucleotides under basic conditions; hydrolysis and ammonolysis with aq. NH3; |
6-(2-Methylamino-benzoylamino)-4-oxo-hexanoic acid (2R,3S,5R)-2-hydroxymethyl-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester
A
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With pyridine; water; acetic acid; hydrazine for 0.0833333h; Ambient temperature; |
5'-O-(4,4'-dimethoxytrityl)-3'-C-(acetyl)thymidine
A
1-((2R,4R,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-hydroxytetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)- dione
B
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With t-butyltin In acetonitrile at 20℃; for 3h; Product distribution; Irradiation; |
1-(5-O-(4,4'-dimethoxytrityl)-3-C-acetyl-2-deoxy-β-D-threo-pentofuranosyl)thymine
A
1-((2R,4R,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-hydroxytetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)- dione
B
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With t-butyltin In acetonitrile at 20℃; for 3h; Product distribution; Irradiation; |
1-(5-O-(4,4'-dimethoxytrityl)-3-C-(1,1-dimethylpropanoyl)-2-deoxy-β-D-threo-pentofuranosyl)thymine
A
1-((2R,4R,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-hydroxytetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)- dione
B
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With t-butyltin In acetonitrile at 20℃; for 1h; Product distribution; Irradiation; |
5'-O-(4,4'-dimethoxytrityl)-3'-C-(2,2-dimethylpropanoyl)thymidine
A
1-((2R,4R,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-hydroxytetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)- dione
B
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With t-butyltin In acetonitrile at 20℃; for 1h; Product distribution; Irradiation; |
1-(5-O-(4,4'-dimethoxytrityl)-3-C-benzoyl-2-deoxy-β-D-threo-pentofuranosyl)thymine
A
1-((2R,4R,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-hydroxytetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)- dione
B
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With t-butyltin In acetonitrile at 20℃; for 2h; Product distribution; Irradiation; |
5'-O-(4,4'-dimethoxytrityl)-3'-C-(benzoyl)thymidine
A
1-((2R,4R,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-hydroxytetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)- dione
B
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With t-butyltin In acetonitrile at 20℃; for 2h; Product distribution; Irradiation; |
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With pyridine for 8h; Hydrolysis; |
levulinic acid
5'-O-(4-4'-dimethoxytrityl)thymidine
5'-O-(4,4'-dimethoxytrityl)-3'-O-levulinoyl-2'-deoxythymidine
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In tetrahydrofuran at 20℃; for 1.5h; | 100% |
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In 1,4-dioxane at 20℃; for 12h; | 99% |
With dmap; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide In 1,4-dioxane for 2.5h; | 98% |
(allyloxy)bis(diisopropylamino)phosphine
5'-O-(4-4'-dimethoxytrityl)thymidine
5'-O-(p,p'-dimethoxytrityl)thymidine 3'-(allyl N,N-diisopropylphosphoramidite)
Conditions | Yield |
---|---|
With 1H-tetrazole; diisopropylamine In acetonitrile at 25℃; for 1.5h; | 100% |
With N,N-diisopropylamine tetrazolide In dichloromethane for 0.166667h; Ambient temperature; |
5'-O-(4-4'-dimethoxytrityl)thymidine
thymidine
Conditions | Yield |
---|---|
With zinc dibromide In nitromethane for 0.0166667h; Ambient temperature; | 100% |
With zinc dibromide In nitromethane Kinetics; Ambient temperature; in various solvent:CH2Cl2, THF, Acetone, Dioxane; other 5'-deoxytritylnucleosides; | 100% |
With β-naphthol In dichloromethane for 0.166667h; Product distribution / selectivity; Irradiation with mercury arc lamp; | 97% |
5'-O-(4-4'-dimethoxytrityl)thymidine
tert-butylchlorodiphenylsilane
1-[(2R,4S,5R)-4-(tert-butyldiphenylsilanyloxy)-5-hydroxymethyltetrahydrofuran-2-yl]-5-methyl-1H-pyrimidine-2,4-dione
Conditions | Yield |
---|---|
Stage #1: 5'-O-(4-4'-dimethoxytrityl)thymidine; tert-butylchlorodiphenylsilane With 1H-imidazole In dichloromethane at 20℃; for 2h; Stage #2: With toluene-4-sulfonic acid In methanol | 100% |
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 72h; | 75% |
With benzoic acid 2) CH2Cl2, MeOH; Multistep reaction; |
(i-Pr2N)2POC(CH3)2CH2CN
5'-O-(4-4'-dimethoxytrityl)thymidine
1,1-dimethyl-2-cyanoethyl 5'-O-(4,4'-dimethoxytrityl)thymidin-3'-yl N,N-diisopropylphosphoramidite
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 24h; Inert atmosphere; | 100% |
succinic acid anhydride
5'-O-(4-4'-dimethoxytrityl)thymidine
triethylamine
5'-O-(4,4'-dimethoxytrityl)-2'-deoxythymidine-3'-O-succinate triethylamine salt
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 16h; Inert atmosphere; | 100% |
Stage #1: succinic acid anhydride; 5'-O-(4-4'-dimethoxytrityl)thymidine With dmap In dichloromethane at 20℃; for 1h; Inert atmosphere; Stage #2: triethylamine In methanol; dichloromethane | 94% |
succinic acid anhydride
5'-O-(4-4'-dimethoxytrityl)thymidine
5'-O-(4,4'-dimethoxytrityl)-2'-deoxythymidine-3'-O-succinate triethylamine salt
Conditions | Yield |
---|---|
Stage #1: succinic acid anhydride; 5'-O-(4-4'-dimethoxytrityl)thymidine With triethylamine In dichloromethane at 20℃; for 16h; Inert atmosphere; Stage #2: triethylammonium dihydrogen phosphate In dichloromethane; water | 100% |
bis(prop-2-en-1-yl)chlorophosphonate
5'-O-(4-4'-dimethoxytrityl)thymidine
Phosphoric acid diallyl ester (2R,3S,5R)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester
Conditions | Yield |
---|---|
With tert-butylmagnesium chloride In tetrahydrofuran for 1h; Ambient temperature; | 99% |
acetic anhydride
5'-O-(4-4'-dimethoxytrityl)thymidine
3'-O-acetyl-5'-O-[bis(4-methoxyphenyl)(phenyl)methyl]-2'-deoxy-3,4-dihydrothymidine
Conditions | Yield |
---|---|
With pyridine at 20℃; Inert atmosphere; | 99% |
With pyridine 1.) 0 deg C, 4 h, 2.) RT, 22 h; | 96% |
In pyridine | 90% |
5'-O-(4-4'-dimethoxytrityl)thymidine
O-(2-cyanoethyl) N,N-diisopropylfluorophosphoramidite
O-[5'-O-(4,4'-dimethoxytrityl)thymidin-3'-yl] O-(2-cyanoethyl) phosphorofluoridite
Conditions | Yield |
---|---|
With chloro-trimethyl-silane In tetrahydrofuran at 20℃; for 1h; | 99% |
With chloro-trimethyl-silane In tetrahydrofuran for 1h; Ambient temperature; | 97% |
With chloro-trimethyl-silane Yield given; |
5'-O-(4-4'-dimethoxytrityl)thymidine
tert-butylchlorodiphenylsilane
1-[(2R,4S,5R)-5-{[bis(4-methoxyphenyl)(phenyl)methoxy]methyl}-4-{[(1,1-dimethylethyl)diphenylsilyl]oxy}tetrahydrofuran-2-yl]-5-methylpyrimidine-2,4(1H,3H)-dione
Conditions | Yield |
---|---|
With 1H-imidazole In N,N-dimethyl-formamide for 24h; | 99% |
Stage #1: 5'-O-(4-4'-dimethoxytrityl)thymidine With 1H-imidazole In dichloromethane for 0.0833333h; Stage #2: tert-butylchlorodiphenylsilane In dichloromethane at 20℃; for 3h; | 99% |
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 12h; | 92% |
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With pyridine; dmap at 20℃; | 99% |
5'-O-(4-4'-dimethoxytrityl)thymidine
hexaethylphosphoric triamide
A
5'-O-dimethoxytrityl thymidine 3'-O-phosphorbisdiethylamidite
Conditions | Yield |
---|---|
1H-tetrazole; diisopropylamine In dichloromethane; water; acetonitrile for 0.25h; Ambient temperature; var. amine catalysts.; Title compound not separated from byproducts; | A 98.5% B 0.5% |
1H-tetrazole In dichloromethane; water; acetonitrile for 0.25h; Ambient temperature; var. amine catalysts.; Title compound not separated from byproducts; | A 71.5% B 25.9% |
tert-butyldimethylsilyl chloride
5'-O-(4-4'-dimethoxytrityl)thymidine
5'-O-(4,4'-dimethoxytrityl)-3'-O-(t-butyldimethylsilyl)-2'-deoxythymidine
Conditions | Yield |
---|---|
With 1H-imidazole In tetrahydrofuran silylation; | 98% |
With 1-methyl-1H-imidazole; iodine In tetrahydrofuran at 20℃; for 1h; | 98% |
With 1-methyl-1H-imidazole; iodine In tetrahydrofuran at 20℃; for 1h; | 98% |
cyclohexylammonium S,S-diphenyl phosphorodithioate
5'-O-(4-4'-dimethoxytrityl)thymidine
Dithiophosphoric acid O-[(2R,3S,5R)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl] ester S,S'-diphenyl ester
Conditions | Yield |
---|---|
With dapsone In pyridine for 4h; Ambient temperature; | 98% |
In pyridine for 6h; | 87% |
With 4,6-dimethoxybenzene-1,3-bis(sulfonyl) chloride In pyridine 1.) 1h, 2.) 7h, RT, 3.) ice cubes, 20 min; | 87% |
dimorpholinophosphinous chloride
5'-O-(4-4'-dimethoxytrityl)thymidine
C39H47N4O9P
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In dichloromethane for 0.5h; | 98% |
p-chlorophenyl N-(p-methoxyphenyl)chlorophosphoramidate
5'-O-(4-4'-dimethoxytrityl)thymidine
(4-Methoxy-phenyl)-phosphoramidic acid (2R,3S,5R)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 4-chloro-phenyl ester
Conditions | Yield |
---|---|
With 1-methyl-1H-imidazole In 1,4-dioxane at 25℃; for 2h; | 98% |
5'-O-(4-4'-dimethoxytrityl)thymidine
O,O'-bis-(4-nitrophenyl) N,N-diisopropylphosphoramidite
O-(5'-O-(4,4'-dimethoxytrityl)thymidin-3'-yl) O-(4-nitrophenyl) N,N-diisopropylphosphoramidite
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile at 20℃; for 0.166667h; | 98% |
With 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile at 20℃; for 0.166667h; | 98% |
With 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile at 20℃; | 95% |
allyloxybis(N,N-dimethylamino)phosphine
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With 1-methylimidazolium trifluoromethanesulfonate In acetonitrile at 25℃; for 1.5h; | 98% |
succinic acid anhydride
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 3h; | 98% |
5'-O-(4-4'-dimethoxytrityl)thymidine
O-[5'-O-(4,4'-dimethoxytrityl)thymidin-3'-yl] O-methyl (O-4-nitrophenyl)-phosphate
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile at 20℃; Inert atmosphere; | 98% |
5'-O-(4-4'-dimethoxytrityl)thymidine
N,N,N',N'-tetraisopropyl-O-[2-[N-isopropyl-N-(4-methoxybenzoyl)amino]ethyl] phosphordiamidite
5'-O-(4,4'-dimethoxytrityl)-3'-O-(N,N-diisopropylamino)-[2-[N-isopropyl-N-(4-methoxybenzoyl)amino]ethoxy]phosphinyl-2'-deoxythymidine
Conditions | Yield |
---|---|
With 1H-tetrazole In dichloromethane; acetonitrile at 20℃; for 2h; | 97.6% |
succinic acid anhydride
5'-O-(4-4'-dimethoxytrityl)thymidine
5’-O-(4,4’-dimethoxytriphenylmethyl)thymidine-3’-O-succinate
Conditions | Yield |
---|---|
With acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene In dichloromethane at 20℃; for 0.75h; Inert atmosphere; | 97% |
With pyridine; dmap at 50℃; for 4h; | |
With pyridine; dmap; triethylamine In dichloromethane for 3h; Ambient temperature; | |
With pyridine; dmap at 20℃; for 20h; | |
With pyridine; dmap |
N,N,N',N'-tetraisopropyl 2-cyanoethylphosphorodiamidite
5'-O-(4-4'-dimethoxytrityl)thymidine
5'-O-(4,4'-dimethoxytrityl)-2'-deoxythymidine-3'-O-[O-(2-cyanoethyl)-N,N'-diisopropylphosphoramidite]
Conditions | Yield |
---|---|
With chloro-trimethyl-silane In tetrahydrofuran for 1h; Ambient temperature; | 97% |
With N,N-diisopropylamine tetrazolide In dichloromethane for 4h; Ambient temperature; | 95% |
With 1H-tetrazole; N-ethyl-N,N-diisopropylamine In dichloromethane for 16h; Ambient temperature; | 95% |
Conditions | Yield |
---|---|
With (iPr)2Et2N In dichloromethane for 0.166667h; Ambient temperature; | 97% |
5'-O-(4-4'-dimethoxytrityl)thymidine
1,1'-carbonyldiimidazole
5'-O-dimethoxytrityl-3'-O-(1-imidazolylcarbonyl)thymidine
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 4h; | 97% |
In acetonitrile for 1h; | 90% |
In acetonitrile for 2h; | |
With dmap In dichloromethane at 20℃; for 14h; | |
With dmap In dichloromethane |
9H-fluoren-9-y1methyl (2-fluoro-2-oxoethyl)carbamate
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With pyridine In dichloromethane for 4h; Ambient temperature; | 97% |
N-(9-fluorenylmethoxycarbonyl)-L-alanyl fluoride
5'-O-(4-4'-dimethoxytrityl)thymidine
Conditions | Yield |
---|---|
With pyridine In dichloromethane for 4h; Ambient temperature; | 97% |
4-Nitrophenyl chloroformate
5'-O-(4-4'-dimethoxytrityl)thymidine
Carbonic acid (2R,3S,5R)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 4-nitro-phenyl ester
Conditions | Yield |
---|---|
With pyridine In dichloromethane Acylation; | 97% |
With pyridine In dichloromethane at 20℃; for 16h; | 62% |
With pyridine In dichloromethane at 0 - 20℃; | 62% |
With pyridine at 80℃; for 20h; |
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