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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720929Generated: October 26, 2026

N-[3-((N-benzyloxycarbonylalanyl)amino)-9,10,11-trimethoxy-6,7-dihydro-5H-dibenzo[a,c]cyclohepten-5-yl]acetamide → N-[3-(alanylamino)-9,10,11-trimethoxy-6,7-dihydro-5H-dibenzo[a,c]cyclohepten-5-yl]acetamide

https://huagongshe.com/reaction/720929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[3-((N-benzyloxycarbonylalanyl)amino)-9,10,11-trimethoxy-6,7-dihydro-5H-dibenzo[a,c]cyclohepten-5-yl]acetamideHCID 53986515—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-[3-(alanylamino)-9,10,11-trimethoxy-6,7-dihydro-5H-dibenzo[a,c]cyclohepten-5-yl]acetamideHCID 6958659665.5%

Reaction Steps

A solution of N-[3-((N-benzyloxycarbonylalanyl)amino)-9,10,11-trimethoxy-6,7-dihydro-5H-dibenzo[a,c]cyclohepten-5-yl]acetamide (70 mg, 0.125 mmol), (prepared as described in Example 1), in ethanol (2 ml) was hydrogenated at atmospheric pressure over 5% palladium on carbon (10 mg) for 2 hours. Ethanol (3 ml) was added and the solution was filtered through diatomaceous earth and the filtrate concentrated under reduced pressure. Trituration with ethyl acetate/diethyl ether gave the title compound (35 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135502B1
Source datasetuspto-grants-2006_11
ORD IDord-18ecf6c6d2cd4e40bc9f4103e3fe8c2d
Source noteuspto-grants-2006_11