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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500843Generated: November 4, 2026

Sodium chloroacetate → 5-Chloro-2-(chloromethyl)-1-[3-(methylsulfonyl)propyl]-1H-benzimidazole

https://huagongshe.com/reaction/1500843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium chloroacetateHCID 23665759—
ReactantTert-butyl 2-amino-4-chlorophenyl(3-(methylsulfonyl)propyl)carbamateHCID 89923659—
SolventHydrochloric AcidHCID 313—
Product5-Chloro-2-(chloromethyl)-1-[3-(methylsulfonyl)propyl]-1H-benzimidazoleHCID 6180818044%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of tert-butyl 2-amino-4-chlorophenyl(3-(methylsulfonyl)propyl)carbamate (320 mg, 0.92 mmol) and sodium chloroacetate (130 mg, 1.1 mmol) in 4 N HCl was heated to 100° C. After overnight stirring, the reaction solution was cooled to RT and concentrated. The residue was diluted with DCM (100 mL) and washed with sat. NaHCO3 (50 mL). The organic layer was dried and concentrated under vacuum. The residue was purified by prep-TLC (DCM/EtOAc=3:1) to give 5-chloro-2-(chloromethyl)-1-(3-(methylsulfonyl)propyl)-1H-benzo[d]imidazole (130 mg, yield: 44%) as pale solid. MS obsd. (ESI+) [(M+H)+]: 321.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206191B2
Source datasetuspto-grants-2015_12
ORD IDord-f546e6ba87dd442a95836d5b46375dab
Source noteuspto-grants-2015_12