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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113509Generated: November 3, 2026

2-Chlorobenzimidazole → tert-Butyl 2-(((1H-benzo[d]imidazol-2-yl)amino)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2113509

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzimidazoleHCID 78572—
Reactanttert-Butyl 2-(aminomethyl)piperidine-1-carboxylateHCID 2756482—
Producttert-Butyl 2-(((1H-benzo[d]imidazol-2-yl)amino)methyl)piperidine-1-carboxylateHCID 7163170030.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

(RS)-2-Aminomethyl-piperidine-1-carboxylic acid tert butyl ester (0.25 g) and 2-chlorobenzimidazole (0.15 g) were combined and warmed to 100° C. for 48 hours. After cooling to room temperature the mixture was column chromatographed (silica gel, ethyl acetate/pentane 1:4—ethyl acetate/pentane 1:1 eluant) to give the title compound (0.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432270B2
Source datasetuspto-grants-2008_10
ORD IDord-68766bc6e99d4d1f997f774f2e0c47a6
Source noteuspto-grants-2008_10