HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol hydrochloride → (3aR*,10aS*)-9-(4-Nitrobenzyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol hydrochloride | HCID 21887872 | — |
| Reactant | (3aR*,10aS*)-9-(4-Nitrobenzyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one | HCID 54563031 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (3aR*,10aS*)-9-(4-Nitrobenzyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one hydrochloride | HCID 70111281 | — |
Reaction Steps
In ethanol was suspended (3aR*,10aS*)-9-(4-Nitrobenzyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]-diazepin-10(1H)-one produced in Working Example 26. To the suspension was added an HCl-ethanol solution, and the mixture was stirred. Resulting crystalline precipitate was collected by filtration, which was washed with ethanol to give the titled compound, m.p. 167°-170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05834463 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-87981e42470b434ab0f2ecf55c5d4f3e |
| Source note | uspto-grants-1998_11 |