HuagongsheHuagongshe Chemistry Print Report · For research reference only
Gyki 52895 → Gyki-53405
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Gyki 52895 | HCID 3539 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Gyki-53405 | HCID 126756 | 85.7% |
Reaction Steps
To a solution of 3.58 g (12.1 mmol) of 1-(4-aminophenyl)-4-methyl-7,8-methylenedioxy-3,4-dihydro-5H-2,3-benzodiazepine in 100 ml of chloroform first 1.68 ml (12.1 mmol) of triethylamine, then under constant ice-cooling and stirring 1.15 ml (12.1 mmol) of acetic anhydride were added. Stirring was continued for additional 2 hours, then the solution was extracted with 3×100 ml of water, the organic layer was dried and evaporated under reduced pressure. The crystalline residue was recrystallized from 40 ml of isopropanol to obtain 3.50 g (85.7%) of the aimed product, m.p. 220°-222° C. After repeated recrystallization the m.p. increased to 223°-225° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05519019 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-51cc0d8d49b146599c0ab0bfa9477575 |
| Source note | uspto-grants-1996_05 |