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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230716Generated: October 25, 2026

Ethanesulfonic acid → n-{2-Tert-butyl-1-[(4,4-difluorocyclohexyl)methyl]-1h-benzimidazol-5-yl}ethanesulfonamide esylate

https://huagongshe.com/reaction/230716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanesulfonic acidHCID 11668—
ReactantEthanesulfonamide, N-(1-((4,4-difluorocyclohexyl)methyl)-2-(1,1-dimethylethyl)-1H-benzimidazol-5-yl)-HCID 11675994—
SolventIsopropyl AcetateHCID 7915—
Productn-{2-Tert-butyl-1-[(4,4-difluorocyclohexyl)methyl]-1h-benzimidazol-5-yl}ethanesulfonamide esylateHCID 16742587—

Reaction Steps

N-{2-tert-butyl-1-[(4,4-difluorocyclohexyl)methyl]-1H-benzimidazol-5-yl}ethanesulfonamide (101 mg) was dissolved in iso-propylacetate (1.5 ml) at 42° C. and ethane sulphonic acid (20 μl, 95%) was added. Crystallisation started immediately. The slurry was left for three days before it was filtered off and washed with iso-propylacetate (3×200 μl). The product was dried at 40° C. under vacuum to yield 61 mg crystalline N-{2-tert-butyl-1-[(4,4-difluorocyclohexyl)methyl]-1H-benzimidazol-5-yl}ethanesulfonamide esylate salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566788B2
Source datasetuspto-grants-2009_07
ORD IDord-63b34ebc74ce45e1b1f7475b5d285e03
Source noteuspto-grants-2009_07