Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489864Generated: October 29, 2026

2-Butenoic acid, 4-oxo-4-phenyl-, ethyl ester → 3-[[1-(ethoxycarbonyl)-3-hydroxy-3-phenyl-propyl]amino]-1-t-butoxycarbonylmethyl-2,3,4,5-tetrahydro-1H-benzazepin-2-one

https://huagongshe.com/reaction/489864

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butenoic acid, 4-oxo-4-phenyl-, ethyl esterHCID 569885—
Reactant1,1-Dimethylethyl ((3S)-3-amino-2-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl)acetateHCID 6350624—
CatalystPalladiumHCID 23938—
SolventTolueneHCID 1140—
Product3-[[1-(ethoxycarbonyl)-3-hydroxy-3-phenyl-propyl]amino]-1-t-butoxycarbonylmethyl-2,3,4,5-tetrahydro-1H-benzazepin-2-oneHCID 22262976—

Reaction Steps

Ethyl 3-benzoylacrylate (13a) (55.6 g, 250 mmoles) is dropped into a solution of (3S)-3-amino-1-t-butoxycarbonylmethyl-2,3,4,5-tetrahydro-1H-benzazepin-2-one (11) (66.2 g, 227 mmoles) in 200 ml of toluene, at room temperature in 1 h. The resulting mixture is left under stirring for 18 h, then added with 10% Pd—C (26 g, 22 mmoles) and hydrogenated at 3 atm for 18 h at room temperature. The solvent is evaporated off and the residue is purified by chromatography (eluent: hexane-ethyl acetate 7:3). A mixture of isomeric products is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06979736B2
Source datasetuspto-grants-2005_12
ORD IDord-a6f7f39591fc4decb95e62663a4c1afd
Source noteuspto-grants-2005_12