HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 20533061, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 20533044 | HCID 20533044 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 20533061 | HCID 20533061 | 59% |
Reaction Steps
10 g 7-chloro-1-(β-chlorethyl)-2-chlormethyl-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepine were reacted in 200 ml methanol with 20 g ammonia gas in a gas autoclave for 16 hours at 90° to 95° C. After heating of the solution under vacuum, the reaction material is yielded in chloroform and washed with dilute aqueous sodium hydroxide solution. After drying and evaporating of the solvent under vacuum the resultive oily reaction product is dissolved in ether. From the concentrated solution, 5 g of 1,2,3,4,4a,5-hexahydro-9-chloro-7-phenyl-pyrazino[1,2-a]-[1,4]benzodiazepine having a melting point of 132°-135° C. are obtained by crystallization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04338314 |
| Source dataset | uspto-grants-1982_07 |
| ORD ID | ord-1d9cb5ae9f11447fb118503e91cf41d6 |
| Source note | uspto-grants-1982_07 |