HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 5-Bromo-5'-[2-(2-bromophenyl)acetamido]-2',5'-dideoxycytidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Bromophenylacetyl chloride | HCID 4138386 | — |
| Reactant | 5'-Amino-5-bromo-2',5'-dideoxycytidine | HCID 53916786 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-5'-[2-(2-bromophenyl)acetamido]-2',5'-dideoxycytidine | HCID 54062532 | — |
Reaction Steps
0.84 ml of a 1M sodium hydroxide solution was added to a solution of 256 mg of 5'-amino-5-bromo-2',5'-dideoxycytidine in 3.3 ml of water. A solution of (2-bromophenyl)acetyl chloride (prepared from 185 mg of the acid) in 5 ml of dichloromethane was added, the mixture was shaken vigorously for 10 minutes and then filtered. The solid was recrystallized from 30 ml of ethanol to give 44 mg of 5-bromo-5'-[2-(2-bromophenyl)acetamido]-2',5'-dideoxycytidine in the form of a white solid of melting point 164°-167° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04851519 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-62c371d9aa714acd8cb584db57fd2ba0 |
| Source note | uspto-grants-1989_07 |