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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633008Generated: October 25, 2026

Benzoyl chloride, 2-chloro-4-(methylsulfonyl)- → Vismodegib

https://huagongshe.com/reaction/633008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 2-chloro-4-(methylsulfonyl)-HCID 11128804—
Reactant4-Chloro-3-(pyridin-2-yl)anilineHCID 40151925—
ProductVismodegibHCID 24776445—

Reaction Steps

Procedure D may also be used to couple 4-chloro-3-(pyridin-2-yl)aniline and 2-chloro-4-(methylsulfonyl)benzoyl chloride to produce 2-chloro-N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(methylsulfonyl)benzamide which is collected by suction filtration and the HCl salt is washed with Et2O (or alternatively with MTBE). This material is freebased using EtOAc/aq NaHCO3 and the organics are dried and concentrated to the solid freebase. This material is then crystallized from acetone:EtOAc (80:20, approx 10 mL/g) which is then finally recrystallized from hot slurry of iPrOAc. 2-chloro-N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(methylsulfonyl)benzamide HCl salt may also be dissolved in distilled water followed by freebasing with 0.5 N NaOH solution (pH to 11) and filtering and vacuum drying the precipitate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321761B2
Source datasetuspto-grants-2016_04
ORD IDord-f71b3d930d7b4833abdee5081bfc1180
Source noteuspto-grants-2016_04