HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052437Generated: October 29, 2026
4-hydroxy-3-methyl-6a,7,8,9-tetrahydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine-6,11-dione → HCID 20301691, compound
https://huagongshe.com/reaction/2052437
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-hydroxy-3-methyl-6a,7,8,9-tetrahydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine-6,11-dione | HCID 323932 | — |
| Solvent | Benzaldehyde dimethyl acetal | HCID 62375 | — |
| Product | HCID 20301691 | HCID 20301691 | 176.8% |
Reaction Steps
2.0 g of 2,3,5,10,11,11a-hexahydro-9-hydroxy-8-methyl-1H-pyrrolo[2,1-C] [1,4]benzodiazepin-5,11-dione was admixed with 300 ml of benzaldehyde dimethyl acetal and heated at 190° to 200° C. for 2 hours with stirring under a stream of nitrogen gas. The liquid reaction mixture was concentrated at 130° to 150° C. under reduced pressure. The concentrate was dissolved in a small quantity of chloroform, passed through a silica gel chromatographic column and eluted with ether. Thus, there was obtained 2.4 g of 6,8,9,10,10a,11-hexahydro-3-methyl-1-phenyl-1H-oxazolo[5,4,3-jk]pyrrolo[2,1-C] [1,4]benzodiazepin-6,11-dione as a colorless crystal. Recrystallization of the resulting product from ether gave a colorless needle-like crystal having a melting point of 158.5° to 162.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04185016 |
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| Source dataset | uspto-grants-1980_01 |
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| ORD ID | ord-cea4cebf6bd44689b28e8eb89e953e6c |
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| Source note | uspto-grants-1980_01 |
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