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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350843Generated: October 25, 2026

1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chloride → 2-(4-tert-Butyl-3-chlorophenoxy)-N-((1R)-1-{3-fluoro-4-[(methylsulfonyl)amino]phenyl}ethyl}acetamide

https://huagongshe.com/reaction/1350843

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chlorideHCID 10986715—
Reactant(4-tert-Butyl-3-chlorophenoxy)acetic acidHCID 21097497—
ReactantN-{4-[(1R)-1-aminoethyl]-2-fluorophenyl}methanesulfonamide hydrochlorideHCID 66841089—
SolventTriethylamineHCID 8471—
Product2-(4-tert-Butyl-3-chlorophenoxy)-N-((1R)-1-{3-fluoro-4-[(methylsulfonyl)amino]phenyl}ethyl}acetamideHCID 1159772830%

Reaction Steps

(4-tert-Butyl-3-chlorophenoxy)acetic acid (121 mg, 0.50 mmol), 2-chloro-1,3-dimethylimidazolinium chloride (CDI) (86 mg, 0.53 mmol), triethylamine (0.5 ml) and N{4-[(1R)-1-aminoethyl]-2-fluorophenyl}methanesulfonamide hydrochloride (134 mg, 0.50 mmol, WO 2005003084A1) were mixed in the same procedure described in Example 2(b) to give 68 mg (30% yield) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214824B2
Source datasetuspto-grants-2007_05
ORD IDord-4adffcdd61c340c9a411d3eaedd176f5
Source noteuspto-grants-2007_05