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Cas Database |
| Name |
Uridine,5-(2-amino-2-oxoethyl)- |
EINECS | N/A |
| CAS No. | 29569-30-0 | Density | 1.653g/cm3 |
| PSA | 169.12000 | LogP | -2.26210 |
| Solubility | N/A | Melting Point |
N/A |
| Formula | C11H15 N3 O7 | Boiling Point | °Cat760mmHg |
| Molecular Weight | 301.256 | Flash Point | °C |
| Transport Information | N/A | Appearance | N/A |
| Safety | Risk Codes | N/A | |
| Molecular Structure |
|
Hazard Symbols | N/A |
| Synonyms |
5-Pyrimidineacetamide,1,2,3,4-tetrahydro-2,4-dioxo-1-b-D-ribofuranosyl- (8CI); 5-Carbamoylmethyluridine; 5-Uridineacetamide |
Article Data | 9 |
Uridine,5-(2-amino-2-oxoethyl)- Synthetic route
- 957-77-7
5-Hydroxy-uridin
- 38821-11-3
2-(triphenylphosphoranylidene)acetamide
- 29569-30-0
5-(carbamoylmethyl)uridine
Conditions
| Conditions | Yield |
|---|---|
| In 1,4-dioxane Heating; | 99% |
- 20299-15-4
2-thio-5-<(methylcarboxy)methyl>uridine
- 29569-30-0
5-(carbamoylmethyl)uridine
Conditions
| Conditions | Yield |
|---|---|
| With ammonium hydroxide In water at 25℃; for 18h; Substitution; | 75% |
- 29428-50-0
5-<(methylcarboxy)methyl>uridine
- 29569-30-0
5-(carbamoylmethyl)uridine
Conditions
| Conditions | Yield |
|---|---|
| With ammonium hydroxide Ambient temperature; | 61.6% |
| With ammonia In methanol for 48h; | |
| With ammonia In methanol for 48h; | |
| With ammonia In methanol at 20℃; for 48h; | |
| With ammonium hydroxide In methanol at 20℃; |
- 58-96-8
uridine
- 29569-30-0
5-(carbamoylmethyl)uridine
Conditions
| Conditions | Yield |
|---|---|
| Multi-step reaction with 6 steps 1: pyridine / 3 h / 60 °C 2: acetic anhydride; acetic acid; bromine / 0 - 20 °C 3: dmap; triethylamine / dichloromethane / 0.5 h / 0 - 20 °C 4: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 20 °C 5: sodium methylate / methanol / 16 h / 50 °C 6: ammonia / methanol / 48 h View Scheme | |
| Multi-step reaction with 6 steps 1: pyridine / 3 h / 60 °C 2: bromine; acetic anhydride; acetic acid / 0 - 20 °C / Sealed tube 3: triethylamine; dmap / dichloromethane / 0.5 h / 0 - 20 °C 4: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 20 °C 5: sodium methylate; methanol / 16 h / 50 °C 6: ammonia / methanol / 48 h View Scheme | |
| Multi-step reaction with 6 steps 1: pyridine / 3 h / 60 °C 2: bromine; acetic anhydride / acetic acid / 0 - 20 °C / Sealed tube 3: dmap; triethylamine / dichloromethane / 0.5 h / 0 - 20 °C 4: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 20 °C 5: sodium methylate / methanol / 16 h / 50 °C 6: ammonia / methanol / 48 h / 20 °C View Scheme |
- 4105-38-8
Tri-O-acetyluridine
- 29569-30-0
5-(carbamoylmethyl)uridine
Conditions
| Conditions | Yield |
|---|---|
| Multi-step reaction with 5 steps 1: acetic anhydride; acetic acid; bromine / 0 - 20 °C 2: dmap; triethylamine / dichloromethane / 0.5 h / 0 - 20 °C 3: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 20 °C 4: sodium methylate / methanol / 16 h / 50 °C 5: ammonia / methanol / 48 h View Scheme | |
| Multi-step reaction with 5 steps 1: bromine; acetic anhydride; acetic acid / 0 - 20 °C / Sealed tube 2: triethylamine; dmap / dichloromethane / 0.5 h / 0 - 20 °C 3: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 20 °C 4: sodium methylate; methanol / 16 h / 50 °C 5: ammonia / methanol / 48 h View Scheme | |
| Multi-step reaction with 5 steps 1: bromine; acetic anhydride / acetic acid / 0 - 20 °C / Sealed tube 2: dmap; triethylamine / dichloromethane / 0.5 h / 0 - 20 °C 3: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 20 °C 4: sodium methylate / methanol / 16 h / 50 °C 5: ammonia / methanol / 48 h / 20 °C View Scheme |
- 105659-31-2, 105659-32-3
5-bromo-2’,3’,5’-tri-O-acetyluridine
- 29569-30-0
5-(carbamoylmethyl)uridine
Conditions
| Conditions | Yield |
|---|---|
| Multi-step reaction with 4 steps 1: dmap; triethylamine / dichloromethane / 0.5 h / 0 - 20 °C 2: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 20 °C 3: sodium methylate / methanol / 16 h / 50 °C 4: ammonia / methanol / 48 h View Scheme | |
| Multi-step reaction with 4 steps 1: triethylamine; dmap / dichloromethane / 0.5 h / 0 - 20 °C 2: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 20 °C 3: sodium methylate; methanol / 16 h / 50 °C 4: ammonia / methanol / 48 h View Scheme | |
| Multi-step reaction with 4 steps 1: dmap; triethylamine / dichloromethane / 0.5 h / 0 - 20 °C 2: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 20 °C 3: sodium methylate / methanol / 16 h / 50 °C 4: ammonia / methanol / 48 h / 20 °C View Scheme |
- 1261157-39-4
5-bromo-N3-benzoyl-2’,3’,5’-tri-O-acetyluridine
- 29569-30-0
5-(carbamoylmethyl)uridine
Conditions
| Conditions | Yield |
|---|---|
| Multi-step reaction with 3 steps 1: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 20 °C 2: sodium methylate / methanol / 16 h / 50 °C 3: ammonia / methanol / 48 h View Scheme | |
| Multi-step reaction with 3 steps 1: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 20 °C 2: sodium methylate; methanol / 16 h / 50 °C 3: ammonia / methanol / 48 h View Scheme | |
| Multi-step reaction with 3 steps 1: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 20 °C 2: sodium methylate / methanol / 16 h / 50 °C 3: ammonia / methanol / 48 h / 20 °C View Scheme |
- 1261157-40-7
N3-benzoyl-2',3',5'-O-triacetoxyuridine-5-malonic acid dimethyl ester
- 29569-30-0
5-(carbamoylmethyl)uridine
Conditions
| Conditions | Yield |
|---|---|
| Multi-step reaction with 2 steps 1: sodium methylate / methanol / 16 h / 50 °C 2: ammonia / methanol / 48 h View Scheme | |
| Multi-step reaction with 2 steps 1: sodium methylate; methanol / 16 h / 50 °C 2: ammonia / methanol / 48 h View Scheme | |
| Multi-step reaction with 2 steps 1: sodium methylate / methanol / 16 h / 50 °C 2: ammonia / methanol / 48 h / 20 °C View Scheme |
- 15715-58-9
triethylamine carbonate
- 29569-30-0
5-(carbamoylmethyl)uridine
Conditions
| Conditions | Yield |
|---|---|
| Stage #1: 5-(carbamoylmethyl)uridine With trimethyl phosphite; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene at 0℃; for 0.166667h; Stage #2: With trichlorophosphate for 2h; Inert atmosphere; Stage #3: triethylamine carbonate Further stages; | 10.52% |
- 15715-58-9
triethylamine carbonate
- 29569-30-0
5-(carbamoylmethyl)uridine
Conditions
| Conditions | Yield |
|---|---|
| Stage #1: 5-(carbamoylmethyl)uridine With N,N,N',N'-tetramethyl-1,8-diaminonaphthalene at 0℃; for 0.166667h; Stage #2: With trichlorophosphate for 2h; Inert atmosphere; Stage #3: triethylamine carbonate Further stages; | 10.52% |
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5-carbamoylmethyluridine
