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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440284Generated: October 30, 2026

Ethanol → HCID 15290905, compound

https://huagongshe.com/reaction/440284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant4-(8-Methyl-9H-1,3-dioxolo(4,5-H)(2,3)benzodiazepin-5-yl)benzenamineHCID 3538—
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
SolventDichloromethaneHCID 6344—
ProductHCID 15290905HCID 1529090571.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

1.0 ml (15 mmol) of benzoyl chloride and 2.1 ml (15 mmol) of triethylamine were added to a solution of 4 g (13.6 mmol) of 1-(4-aminophenyl)-4-methyl-7,8-methylenedioxy-5H-2,3-benzodiazepine in dichloromethane and the reaction mixture was stirred at 25° C. for 24 hours. The solution was extracted with 3×30 ml of water, 3×20 ml of a 4% aqueous sodium hydroxide solution and finally with 2×30 ml of distilled water. The organic layer was dried, evaporated under reduced pressure, then the crystalline residue was treated with 20 ml of hot ethanol to obtain 3.97 g of raw product, m.p. 242°-243° C. This raw product was repeatedly treated with 20 ml of hot ethanol, next day it was filtered at 0°-5° C., washed with 3×3 ml of ethanol and dried at 100° C. to yield 3.85 g (71.3%) of the pure aimed product, m.p. 246°-247° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05519019
Source datasetuspto-grants-1996_05
ORD IDord-57d064aa07124fe5884860707d5064fd
Source noteuspto-grants-1996_05