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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632779Generated: October 26, 2026

Ethyl alpha-oxobenzenebutanoate → 3-[N-(1-carboethoxy-3-phenylpropyl)amino]-5-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one

https://huagongshe.com/reaction/1632779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl alpha-oxobenzenebutanoateHCID 562087—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-Amino-5-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2-oneHCID 20442332—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
Product3-[N-(1-carboethoxy-3-phenylpropyl)amino]-5-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-oneHCID 20442330—

Reaction Steps

The 3-amino-5-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2-one (0.267 g) is dissolved in 5 ml of methanol and 0.288 g of ethyl 2-oxo-4-phenylbutyrate is added. This is followed by the addition of a solution of 88 mg of sodium cyanoborohydride in 3 ml of methanol and 0.8 ml of glacial acetic acid. The reaction is stirred overnight under nitrogen and concentrated. The residue is dissolved in 20 ml of methylene chloride and washed with 10 ml of cold saturated sodium carbonate. After drying over magnesium sulfate the solution is concentrated and the residue purified to give 3-[N-(1-carboethoxy-3-phenylpropyl)amino]-5-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2(2H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04477464
Source datasetuspto-grants-1984_10
ORD IDord-917fe34274cf4ee5ac1512e28f4bf307
Source noteuspto-grants-1984_10