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inquiryformaldehyd
cytidine 5'-(dihydrogen phosphate)
5-hydroxymethyl-2'-deoxycytidine 5'-monophosphate
Conditions | Yield |
---|---|
in Gegenwart eines Enzympraeparats aus virusinfizierten Escherichiacoli-Zellen; |
5-methyl-2′-deoxycytidine 5′-monophosphate
A
5-hydroxymethyl-2'-deoxycytidine 5'-monophosphate
B
5-formyl-2'-deoxycytidine 5'-monophosphate
Conditions | Yield |
---|---|
With sodium persulfate In water at 75℃; for 3h; sodium phosphate buffer pH 7.0; | A 15 % Spectr. B 10 % Spectr. |
With sodium persulfate; buffer pH=7.0 In water at 75℃; for 4h; | A 12 % Spectr. B 8 % Spectr. |
5-acetoxymethyl-3',5'-di-O-tert-butyldimethylsilyl-2'-deoxycytidine
5-hydroxymethyl-2'-deoxycytidine 5'-monophosphate
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: trichlorophosphate; trimethyl phosphite / 2 h / 0 °C 2: trifluoroacetic acid / water / 1 h / 20 °C 3: potassium carbonate; water / methanol / 1 h / 20 °C View Scheme |
3',5'-O-di(tert-butyldimethylsilyl)thymidine
5-hydroxymethyl-2'-deoxycytidine 5'-monophosphate
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1.1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 1.5 h / 80 °C 2.1: 0.5 h / 40 °C 3.1: p-toluenesulfonyl chloride; N-methylcyclohexylamine; triethylamine / 4 h 3.2: 0.5 h 4.1: trichlorophosphate; trimethyl phosphite / 2 h / 0 °C 5.1: trifluoroacetic acid / water / 1 h / 20 °C 6.1: potassium carbonate; water / methanol / 1 h / 20 °C View Scheme |
5-hydroxymethyl-2'-deoxycytidine 5'-monophosphate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: trifluoroacetic acid / water / 1 h / 20 °C 2: potassium carbonate; water / methanol / 1 h / 20 °C View Scheme |
5-hydroxymethyl-2'-deoxycytidine 5'-monophosphate
Conditions | Yield |
---|---|
With water; potassium carbonate In methanol at 20℃; for 1h; |
3′,5′-bis-O-(tert-butyldimethylsilyl)-5-bromomethyl-2'-deoxyuridine
5-hydroxymethyl-2'-deoxycytidine 5'-monophosphate
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: 0.5 h / 40 °C 2.1: p-toluenesulfonyl chloride; N-methylcyclohexylamine; triethylamine / 4 h 2.2: 0.5 h 3.1: trichlorophosphate; trimethyl phosphite / 2 h / 0 °C 4.1: trifluoroacetic acid / water / 1 h / 20 °C 5.1: potassium carbonate; water / methanol / 1 h / 20 °C View Scheme |
5-acetoxymethyl-3',5'-di-O-tert-butyldimethylsilyl-2'-deoxyuridine
5-hydroxymethyl-2'-deoxycytidine 5'-monophosphate
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: p-toluenesulfonyl chloride; N-methylcyclohexylamine; triethylamine / 4 h 1.2: 0.5 h 2.1: trichlorophosphate; trimethyl phosphite / 2 h / 0 °C 3.1: trifluoroacetic acid / water / 1 h / 20 °C 4.1: potassium carbonate; water / methanol / 1 h / 20 °C View Scheme |
Conditions | Yield |
---|---|
With triphenylphosphine; 2-Aminophenyl disulfide In dimethyl sulfoxide at 20℃; for 8h; | 94% |
5-hydroxymethyl-2'-deoxycytidine 5'-monophosphate
5-hydroxymethyl-2'-deoxycytidine-5’-triphosphate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 2-Aminophenyl disulfide; triphenylphosphine / dimethyl sulfoxide / 8 h / 20 °C 2: tris(tetra-n-butylammonium) hydrogen pyrophosphate; 4,5-dicyano-1H-imidazole / 6 h / 20 °C View Scheme |
5-hydroxymethyl-2'-deoxycytidine 5'-monophosphate
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 2-Aminophenyl disulfide; triphenylphosphine / dimethyl sulfoxide / 8 h / 20 °C 2: tris(tetra-n-butylammonium) hydrogen pyrophosphate; 4,5-dicyano-1H-imidazole / 6 h / 20 °C 3: 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene / dichloromethane; water; tert-butyl alcohol / 48 h / 20 °C View Scheme |
5-hydroxymethyl-2'-deoxycytidine 5'-monophosphate
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 2-Aminophenyl disulfide; triphenylphosphine / dimethyl sulfoxide / 8 h / 20 °C 2: manganese(IV) oxide / methanol / 24 h / 50 °C 3: tris(tetra-n-butylammonium) hydrogen pyrophosphate; 4,5-dicyano-1H-imidazole / 6 h / 20 °C View Scheme |
5-hydroxymethyl-2'-deoxycytidine 5'-monophosphate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 2-Aminophenyl disulfide; triphenylphosphine / dimethyl sulfoxide / 8 h / 20 °C 2: manganese(IV) oxide / methanol / 24 h / 50 °C View Scheme |
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