Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633206Generated: October 30, 2026

4-Chloro-3-(pyridin-2-yl)aniline → HCID 58614767, compound

https://huagongshe.com/reaction/633206

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-3-(pyridin-2-yl)anilineHCID 40151925—
ReactantHCID 66878142HCID 66878142—
ProductHCID 58614767HCID 58614767—

Reaction Steps

140 mg of (R)-propylene oxide was reacted with methyl 2-chloro-4-mercaptobenzoate via Procedure S to afford (R)-methyl 2-chloro-4-(2-hydroxypropylthio)benzoate. 435 mg of (R)-methyl-2-chloro-4-(2-hydroxypropylthio)benzoate was hydrolyzed via Procedure M to give (R)-2-chloro-4-(2-hydroxypropylthio)benzoic acid. 403 mg of (R)-2-chloro-4-(2-hydroxypropylthio)benzoic acid was reacted via Procedure R to give (R)-2-chloro-4-(2-hydroxypropylsulfonyl)benzoic acid. 298 mg of 4-chloro-3-(pyridine-2-yl)aniline was coupled to (R)-2-chloro-4-(2-hydroxypropylsulfonyl)benzoic acid via Procedure G. The product was purified on reverse phase HPLC to yield (R)-2-chloro-N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(2-hydroxypropylsulfonyl)benzamide. MS (Q1) 465.1 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321761B2
Source datasetuspto-grants-2016_04
ORD IDord-622dd87697a145d1ab330f2f5bb5fced
Source noteuspto-grants-2016_04