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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194978Generated: November 1, 2026

3-Amino-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-1-t-butyl acetate → HCID 70396000, compound

https://huagongshe.com/reaction/1194978

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepin-1-t-butyl acetateHCID 3674165—
ReactantEthyl 6-(1-benzyloxycarbonyl-4-piperidyl)-2-methanesulfonyloxyhexanoateHCID 13652732—
SolventEthyl AcetateHCID 8857—
ProductHCID 70396000HCID 7039600052.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 1.75 g of tert-butyl 3-amino-2-oxo-2,3,4,5-tetrahydro-1H-1-benzazepine-1-acetate and 1.1 g of ethyl 6-(1-benzyloxycarbonyl-4-piperidyl)-2-methanesulfonyloxyhexanoate is heated at 90° C. for 24 hours. After cooling, the reaction solution is diluted with 200 ml of ethyl acetate, and the resulting solution is washed with 30 ml of 5% aqueous phosphoric acid and water, successively, and dried over anhydrous magnesium sulfate. After the solvent is distilled off under reduced pressure, the residue is separated and purified by silica gel colum chromatography (hexane:ethyl acetate=2:1), whereby the first fraction yields 0.8 g of tert-butyl 3(RS)-[5-(1-benzyloxycarbonyl-4-piperidyl)-1(SR)-ethoxycarbonylpentyl]amino-2,3,4,5-tetrahydro-1H-1-benzazepine-1-acetate as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816466
Source datasetuspto-grants-1989_03
ORD IDord-345a11a116504ae48cc235d9c73427e3
Source noteuspto-grants-1989_03