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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979413Generated: October 29, 2026

Triethylamine → 1-[1-(2-toluoylmethyl)-2-oxo-5-(3-methyl-2-butenoyl)-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepin-3-yl]-3-(3-ethoxycarbonylphenyl)urea

https://huagongshe.com/reaction/1979413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl 3-aminobenzoateHCID 11400—
ReactantTriphosgeneHCID 94429—
Reactant1-(2-toluoylmethyl)-2-oxo-3-amino-5-(3-methyl-2-butenoyl)-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepineHCID 21201651—
SolventTetrahydrofuranHCID 8028—
Product1-[1-(2-toluoylmethyl)-2-oxo-5-(3-methyl-2-butenoyl)-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepin-3-yl]-3-(3-ethoxycarbonylphenyl)ureaHCID 21201898106%

Reaction Steps

Ethyl 3-aminobenzoate (290 mg) was dissolved in tetrahydrofuran (60 m), under ice-cooling triphosgene (175 mg) was added, triethylamine (151 μl) was added thereto five times every 3 minutes,a solution of 1-(2-toluoylmethyl)-2-oxo-3-amino-5-(3-methyl-2-butenoyl)-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine (647 mg) in tetrahydrofuran (5 ml) was subsequently added, and the mixture was allowed to come to room temperature and stirred for 2 hours and 40 minutes. The reaction mixture was concentrated under reduced pressure, water was added, and extracted with methylene chloride. The organic layer was successively washed with 1N hydrochloric acid and saturated aqueous sodium bicarbonate, dried over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography(chloroform:ethyl acetate=5:1), to thereby obtain 373 mg of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06239131B1
Source datasetuspto-grants-2001_05
ORD IDord-dc1aa83df99342ccb513b29935481a06
Source noteuspto-grants-2001_05