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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633213Generated: October 31, 2026

Methyl 4-sulfanylbenzoate → HCID 66878049, compound

https://huagongshe.com/reaction/633213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-sulfanylbenzoateHCID 237573—
Reactant3-(Bromomethyl)pyridine hydrobromideHCID 12707037—
ProductHCID 66878049HCID 66878049—

Reaction Steps

1 g of 3-(bromomethyl)pyridine hydrobromide was reacted with methyl 4-mercaptobenzoate via Procedure Q to afford methyl 4-(pyridin-3-ylmethylthio)benzoate. 980 mg of methyl 4-(pyridin-3-ylmethylthio)benzoate was reacted via Procedure R to give methyl 4-(pyridin-3-ylmethylsulfonyl)benzoate. 760 mg of methyl 4-(pyridin-3-ylmethylsulfonyl)benzoate was hydrolyzed via Procedure M to give 4-(pyridin-3-ylmethylsulfonyl)benzoic acid. 60 mg of 4-chloro-3-(pyridin-2-yl)aniline was coupled to 4-(pyridin-3-ylmethylsulfonyl)benzoic acid via Procedure G. The product was purified on reverse phase HPLC to yield N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(pyridin-3-ylmethylsulfonyl)benzamide. MS (Q1) 464.1 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321761B2
Source datasetuspto-grants-2016_04
ORD IDord-d4793dbfdcf9426e934b28734345b351
Source noteuspto-grants-2016_04