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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968835Generated: November 1, 2026

Thiophene → 3-(2-Amino-5-benzoyl-benzylamino)-N-cyclohexyl-N-methyl-propionamide

https://huagongshe.com/reaction/1968835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
Reactant3-(5-Benzoyl-2-nitro-benzylamino)-N-cyclohexyl-N-methyl-propionamideHCID 17756485—
CatalystPlatinumHCID 23939—
SolventMethanolHCID 887—
Product3-(2-Amino-5-benzoyl-benzylamino)-N-cyclohexyl-N-methyl-propionamideHCID 58625111—

Reaction Steps

3-(5-Benzoyl-2-nitro-benzylamino)-N-cyclohexyl-N-methyl-propionamide (0.01 mol) was converted into its corresponding free base. A mixture of the free base (0.01 mol) in methanol (200 mL) was hydrogenated under atmospheric conditions, with 5% Pt/C (2 g) as a catalyst in the presence of 4% thiophene solution (1 mL). After uptake of H2 (3 equiv.), the catalyst was filtered off and the filtrate was evaporated. Toluene was added to the residue, then evaporated again to yield the title compound as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426429B2
Source datasetuspto-grants-2013_04
ORD IDord-e0253f2d706a4a8bb4af44a74c3e945c
Source noteuspto-grants-2013_04