HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → HCID 54105642, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | HCID 54231756 | HCID 54231756 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 54105642 | HCID 54105642 | — |
Reaction Steps
5.8 g (18.2 mmol) of (S)-7-chloro-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxylic acid are heated to 230°. After completion of the carbon dioxide evolution, the melt is treated with ethyl acetate. The solid material is filtered off under suction and dried. There is obtained (S)-7-chloro-11,12,13,13a-tetrahydro-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepin-9-one of melting point 216°-217°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04352818 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-f80178c66351421f9f8f58658c049ace |
| Source note | uspto-grants-1982_10 |