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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951148Generated: November 4, 2026

3-Bromo-4-chlorobenzoic acid → 3-bromo-4-chloro-N-{(3RS,4SR)-4-(3,4-dichloro-phenyl)-1-[1-(1-methyl-cyclopropanecarbonyl)-piperidine-4-carbonyl]-pyrrolidin-3-yl}-N-methyl-benzamide

https://huagongshe.com/reaction/1951148

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-4-chlorobenzoic acidHCID 2735544—
Reactant[(3SR,4RS)-3-(3,4-Dichloro-phenyl)-4-methylamino-pyrrolidin-1-yl]-[1-(1-methyl-cyclopropanecarbonyl)-piperidin-4-yl]-methanoneHCID 67025815—
Product3-bromo-4-chloro-N-{(3RS,4SR)-4-(3,4-dichloro-phenyl)-1-[1-(1-methyl-cyclopropanecarbonyl)-piperidine-4-carbonyl]-pyrrolidin-3-yl}-N-methyl-benzamideHCID 67025699—

Reaction Steps

In analogy to the procedure described for the synthesis of example 97, the title compound 3-bromo-4-chloro-N-{(3RS,4SR)-4-(3,4-dichloro-phenyl)-1-[1-(1-methyl-cyclopropanecarbonyl)-piperidine-4-carbonyl]-pyrrolidin-3-yl}-N-methyl-benzamide was prepared from {4-[(3SR,4RS)-3-(3,4-dichloro-phenyl)-4-methylamino-pyrrolidine-1-carbonyl]-piperidin-1-yl}-(1-methyl-cyclopropyl)-methanone using 3-bromo-4-chlorobenzoic acid instead of 4-chloro-3-(trifluoromethyl)benzoic acid and was obtained as a colorless oil. MS m/e: 656.0 [M]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404679B2
Source datasetuspto-grants-2013_03
ORD IDord-94c5fd9f115b4dbf849bbb86d9bc0668
Source noteuspto-grants-2013_03