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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242741Generated: October 27, 2026

1-[(Tert-butoxy)carbonyl]piperidine-2-carboxylic acid → n-[(1r)-1-[(4-Chlorophenyl)methyl]-2-(4-{2-[(methylsulfonyl)amino]phenyl}piperazinyl)-2-oxoethyl](1-methyl(2-piperidyl))carboxamide

https://huagongshe.com/reaction/1242741

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[(Tert-butoxy)carbonyl]piperidine-2-carboxylic acidHCID 581831—
ReactantHCID 58714305HCID 58714305—
Productn-[(1r)-1-[(4-Chlorophenyl)methyl]-2-(4-{2-[(methylsulfonyl)amino]phenyl}piperazinyl)-2-oxoethyl](1-methyl(2-piperidyl))carboxamideHCID 21060071—
ProductHCID 69077408HCID 69077408—

Reaction Steps

tert-Butyl 2-{N-[(1R)-1-[(4-chlorophenyl)methyl]-2-(4-{2-[(methylsulfonyl)amino]phenyl}piperazinyl)-2-oxoethyl]carbamoyl}piperidinecarboxylate was prepared according to the procedure described in Preparation V by using piperidine-1,2-dicarboxylic acid 1-tert-butyl ester (Aldrich) (82 mg, 0.36 mmol) and (2R)-2-Amino-3-(4-chlorophenyl)-1-(4-{2-[(methylsulfonyl}-amino]phenyl}piperazinyl)propan-1-one. The desired compound was isolated as a white solid (106 mg). MS (ESI, pos. ion) m/z: 648 (M+H); (ESI, neg. ion) m/z: 646 (M−H). Calc'd for C31H42ClN5O6S: 647.25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115607B2
Source datasetuspto-grants-2006_10
ORD IDord-d1807ea4c4f44b92b848c5ee7ac27181
Source noteuspto-grants-2006_10