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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268178Generated: October 29, 2026

HCID 54110954, compound → HCID 53863065, compound

https://huagongshe.com/reaction/268178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54110954HCID 54110954—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 53863065HCID 53863065—

Reaction Steps

A mixture of 6.44 g. of 7-benzyloxy-1,2,3,5,10,11a- hexahydro-10-methyl-11H-pyrrolo[2,1-c] [1,4]benzodiazepin-11- one, 200 ml. of ethanol and 1.0 g. of 10% palladium-on-carbon catalyst is shaken in a Parr hydrogenator under about 3 atmospheric of hydrogen pressure until the theoretical amount of hydrogen is absorbed. The catalyst is filtered off and the mother liquor is concentrated to remove the solvent. The residue is purified by partition chromatography on a diatomaceous earth column using a heptane/methyl cellosolve solvent system to yield pure 1,2,3,5,10,11a-hexahydro-7-hydroxy- 10-methyl-11H-pyrrolo[2,1-c] [1,4]benzodiazepin-11-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03947408
Source datasetuspto-grants-1976_03
ORD IDord-38834a805c084876aa43b7de5190402d
Source noteuspto-grants-1976_03