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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740057Generated: November 1, 2026

Ethanol → (4-amino-3-methoxy-phenyl)[10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-10-yl]methanone

https://huagongshe.com/reaction/1740057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTetrahydrofuranHCID 8028—
Reactant10,11-dihydro-10-(4-nitro-3-methoxybenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepineHCID 10713740—
SolventDichloromethaneHCID 6344—
Product(4-amino-3-methoxy-phenyl)[10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-10-yl]methanoneHCID 10806563—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 0.91 g of 10,11-dihydro-10-(4-nitro-3-methoxybenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine, 4.51 g of SnCl 2.2H2O, 6 ml of ethyl alcohol, 6 ml of tetrahydrofuran and 16 ml of methylene chloride is stirred at 50° C. for 2 hours. The solvents are evaporated in vacuo and the residue dissolved in 80 ml of ethyl acetate. The solution is treated with 50 ml of 1N NaOH with stirring for 30 minutes. The resulting suspension is filtered through diatomaceous earth.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05968930
Source datasetuspto-grants-1999_10
ORD IDord-92d9e5f99d1a4924b00d4c7580e1ef5c
Source noteuspto-grants-1999_10