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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350848Generated: October 25, 2026

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

https://huagongshe.com/reaction/1350848

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chlorideHCID 10986715—
Reactant(4-tert-Butyl-3-fluorophenoxy)acetic acidHCID 21097504—
ReactantN-{4-[(1R)-1-aminoethyl]-2-methylphenyl)methanesulfonamide hydrochlorideHCID 21097519—
SolventTriethylamineHCID 8471—
Product(4-tert-butyl-3-fluorophenoxy)-N-((1R)-1-{3-methyl-4-[(methylsulfonyl)amino]phenyl}ethyl)acetamideHCID 1159020444%

Reaction Steps

(4-tert-Butyl-3-fluorophenoxy) acetic acid (153 mg, 0.68 mmol), 2-chloro-1,3-dimethylimidazolinium chloride (CDI) (110 mg, 0.68 mmol), triethylamine (0.5 ml) and N-{4-[(1R)-1-aminoethyl]-2-methylphenyl}methanesulfonamide hydrochloride (180 mg, 0.68 mmol) were mixed in the same procedure described in Example 2(b) to give 129 mg (44% 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-7f72634798ab4ae1b9943a209c7eb766
Source noteuspto-grants-2007_05