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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-hydroxy-3-methyl-6a,7,8,9-tetrahydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine-6,11-dioneHCID 323932—
SolventBenzaldehyde dimethyl acetalHCID 62375—
ProductHCID 20301691HCID 20301691176.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04185016
Source datasetuspto-grants-1980_01
ORD IDord-cea4cebf6bd44689b28e8eb89e953e6c
Source noteuspto-grants-1980_01