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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190664Generated: October 29, 2026

N-(3-tert-Butyl-phenyl)-4-piperidin-4-yl-benzamide → 4-{4-[4-(3-tert-Butyl-phenylcarbamoyl)-phenyl]-piperidine-1-carbonyl}-cyclohexanecarboxylic acid

https://huagongshe.com/reaction/2190664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-tert-Butyl-phenyl)-4-piperidin-4-yl-benzamideHCID 59317976—
Reactant(1S,2S)-2-{4-[5-(3-tert-butyl-phenylcarbamoyl)-pyridin-2-yl]-piperazine-1-carbonyl}-cyclopentanecarboxylic acidHCID 59317991—
ReactantHCID 178525735HCID 178525735—
Product4-{4-[4-(3-tert-Butyl-phenylcarbamoyl)-phenyl]-piperidine-1-carbonyl}-cyclohexanecarboxylic acidHCID 59318168—

Reaction Steps

4-{4-[4-(3-tert-Butyl-phenylcarbamoyl)-phenyl]-piperidine-1-carbonyl}-cyclohexanecarboxylic acid was prepared from N-(3-tert-butyl-phenyl)-4-piperidin-4-yl-benzamide and trans-1,4-cyclohexane dicarboxylic acid monobenzyl ester in a manner similar to the one described in the synthesis of (1S,2S)-2-{4-[5-(3-tert-butyl-phenylcarbamoyl)-pyridin-2-yl]-piperazine-1-carbonyl}-cyclopentanecarboxylic acid above. LCMS calcd for C30H38N2O4 (m/e) 490, obsd 491 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324385B2
Source datasetuspto-grants-2012_12
ORD IDord-b963578cf5eb4e98b37907f7d5f671be
Source noteuspto-grants-2012_12