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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440799Generated: October 29, 2026

4-(8-Methyl-9H-1,3-dioxolo(4,5-H)(2,3)benzodiazepin-5-yl)benzenamine → 1-(4-Phenylcarbamoylaminophenyl)-4-methyl-7,8-methylenedioxy-5H-2,3-benzodiazepine

https://huagongshe.com/reaction/440799

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(8-Methyl-9H-1,3-dioxolo(4,5-H)(2,3)benzodiazepin-5-yl)benzenamineHCID 3538—
ReactantPhenyl isocyanateHCID 7672—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product1-(4-Phenylcarbamoylaminophenyl)-4-methyl-7,8-methylenedioxy-5H-2,3-benzodiazepineHCID 1904068878.6%

Reaction Conditions

Temperature25 °C

Reaction Steps

0.22 ml (2.04 mmol) of phenyl isocyanate was added to a solution of 0.50 g (1.7 mmol) of 1-(4-aminophenyl)-4-methyl-7,8-methylenedioxy-5H-2,3-benzodiazepine in 4 ml of dimethylformamide and the reaction mixture was stirred at 25° C. for one hour. Then it was diluted with 20 ml of diethyl ether and filtered at 5° C. The crystals were washed with 2×5 ml of diethyl ether and dried at 60°-100° C. The resulting 0.70 g of raw product, m.p. 239°-240° C. (sintering at 180° C. was refluxed in 15 ml of ethanol, filtered after cooling, washed with 3×1 ml of ethanol and dried at 100° C. to yield 0.55 g (78.6%) of the aimed product, m.p. 240°-241° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521174
Source datasetuspto-grants-1996_05
ORD IDord-84fd86c699e14e54bb90eb68853d552b
Source noteuspto-grants-1996_05