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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736946Generated: October 30, 2026

benzyl 4-(1-{(S)-2-(4-amino-3-chloro-5-trifluoromethyl-benzyl)-4-oxo-4-[4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidin-1-yl]-butyryl}-piperidin-4-yl)-piperazin-1-carboxylate → (S)-2-(4-amino-3-chloro-5-trifluoromethyl-benzyl)-4-[4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidin-1-yl]-1-(4-piperazin-1-yl-piperidin-1-yl)-butan-1,4-dione

https://huagongshe.com/reaction/736946

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbenzyl 4-(1-{(S)-2-(4-amino-3-chloro-5-trifluoromethyl-benzyl)-4-oxo-4-[4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidin-1-yl]-butyryl}-piperidin-4-yl)-piperazin-1-carboxylateHCID 68591073—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product(S)-2-(4-amino-3-chloro-5-trifluoromethyl-benzyl)-4-[4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidin-1-yl]-1-(4-piperazin-1-yl-piperidin-1-yl)-butan-1,4-dioneHCID 57848411—

Reaction Steps

100 mg Raney nickel were added to a solution of 250 mg (0.30 mmol) benzyl 4-(1-{(S)-2-(4-amino-3-chloro-5-trifluoromethyl-benzyl)-4-oxo-4-[4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidin-1-yl]-butyryl}-piperidin-4-yl)-piperazin-1-carboxylate in 30 mL MeOH and the reaction mixture was stirred for 5 h at RT and 50 psi H2. To complete the reaction another 100 mg of Raney nickel were added and the mixture was stirred for a further 10 h at RT. The catalyst was suction filtered, the solvent eliminated i. vac. and the residue purified by HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595312B2
Source datasetuspto-grants-2009_09
ORD IDord-6d0badaa00874021a72cd23255e64e12
Source noteuspto-grants-2009_09