HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 1-Ethoxycarbonylmethyl-N4-benzoyl cytosine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178522337 | HCID 178522337 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Ethoxycarbonylmethyl-N4-benzoyl cytosine | HCID 12009709 | 54% |
Reaction Steps
To a stirred suspension of 6 (1.92 g, 9 mmol) in dry DMF (100 mL) at 0° C., NaH (0.43 g, 18 mmol) was added and the mixture was stirred at room temperature for 1 h. Ethyl bromoacetate (1.5 g, 9 mmol) was added dropwise at 0° C. and stirred for 1 h. Methanol (2 mL) was added to quench the reaction, and the solvents were removed under reduced pressure. The residue obtained was dissolved in DCM, washed with water (3×50 mL), dried over Na2SO4, and the solvent was evaporated to give 7 as a white solid (1.38 g, 54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859490B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-d0666185efee491aa6927ea378cc951a |
| Source note | uspto-grants-2014_10 |