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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500875Generated: November 3, 2026

4-(5-Chloro-2-chloromethyl-benzoimidazol-1-yl)-piperidine-1-carboxylic acid tert-butyl ester → 1-{[5-Chloro-1-(piperidin-4-yl)-1H-benzimidazol-2-yl]methyl}-3-(methylsulfonyl)-1H-indazole

https://huagongshe.com/reaction/1500875

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(5-Chloro-2-chloromethyl-benzoimidazol-1-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 118114330—
Reactant3-methanesulfonyl-1H-indazoleHCID 178504856—
ReactantHCID 178504858HCID 178504858—
Product1-{[5-Chloro-1-(piperidin-4-yl)-1H-benzimidazol-2-yl]methyl}-3-(methylsulfonyl)-1H-indazoleHCID 72950642—

Reaction Steps

The title compound was prepared in analogy to Example 2-13 by using 4-(5-chloro-2-chloromethyl-benzoimidazol-1-yl)-piperidine-1-carboxylic acid tert-butyl ester and 3-methanesulfonyl-1H-indazole instead of 3-(5-chloro-2-chloromethyl-benzoimidazol-1-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester and 3-methanesulfonyl-1H-pyrazolo[3,4-c]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206191B2
Source datasetuspto-grants-2015_12
ORD IDord-c46d7ac69aea4b4bb2c3ac7cfa8f9c7e
Source noteuspto-grants-2015_12