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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633205Generated: October 26, 2026

(R)-1,2-Epoxypropane → (R)-methyl 2-chloro-4-(2-hydroxypropylthio)benzoate

https://huagongshe.com/reaction/633205

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-1,2-EpoxypropaneHCID 146261—
ReactantMethyl 2-chloro-4-mercaptobenzoateHCID 66877363—
Product(R)-methyl 2-chloro-4-(2-hydroxypropylthio)benzoateHCID 66877954—

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-e0a684eb795845ec9086059e644ac088
Source noteuspto-grants-2016_04