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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810192Generated: October 31, 2026

5-Bromo-2-methyl-1H-benzo[d]imidazole → HCID 58107460, compound

https://huagongshe.com/reaction/1810192

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-methyl-1H-benzo[d]imidazoleHCID 610979—
Reactant4-chloro-N-methoxy-N-methyl-3-sulfamoyl-benzamideHCID 58107399—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58107460HCID 58107460—

Reaction Steps

A solution of 0.303 g of 6-bromo-2-methyl-1H-benzoimidazole in tetrahydrofuran (20 mL) is cooled to −50° C. and treated with 2.7 mL of tert-butyllithium (1.5 M in pentane). After 2 h at −50° C. the reaction mixture is treated with 0.12 g of 4-chloro-N-methoxy-N-methyl-3-sulfamoyl-benzamide in tetrahydrofuran (10 mL). After 3 h the mixture is quenched with saturated aqueous ammonium chloride, taken up in ethyl acetate, and washed with saturated aqueous sodium chloride. The organics are dried (magnesium sulfate), concentrated and purified by silica gel chromatography (98:2 methylene chloride/methanol) to give 2-chloro-5-(2-methyl-3H-benzoimidazole-5-carbonyl)-benzenesulfonamide. MS (m/z): 348 (M−1); Rf 0.30 (9:1 methylene chloride/methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362063B2
Source datasetuspto-grants-2013_01
ORD IDord-73cba3e20b064e1fa3fc5603d7855bbf
Source noteuspto-grants-2013_01