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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505781Generated: November 2, 2026

Citric Acid → HCID 71267549, compound

https://huagongshe.com/reaction/1505781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantAcetyl chlorideHCID 6367—
ReactantDiisopropylethylamineHCID 81531—
ReactantTetrahydrofurane dichloromethaneHCID 21919333—
ReactantHCID 90229257HCID 90229257—
ProductHCID 71267549HCID 71267549—

Reaction Steps

A mixture of 2-(hydroxymethyl)-6-({[2-(trifluoromethyl)phenyl]carbonyl}amino)-1H-benzimidazole-4-carboxylic acid (50 mg) and N,N-diisopropylethylamine (49 μL) in methylene chloride-THF (1:1) (2 mL) was stirred under ice-cooling, acetyl chloride (19 μL) was added, and it was stirred at room temperature overnight. The reaction mixture was poured into a cold 10% aqueous citric acid solution, and extracted with ethyl acetate. The organic layer was separated, washed with brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was dissolved in DMF (3 mL), HBTU (65 mg) and triethylamine (24 μL) were added, and it was stirred at room temperature. To the mixture was added 3-chloro-2-methylaniline (16 μL) and it was stirred overnight. The reaction mixture was poured into ice water, and extracted with ethyl acetate. The organic layer was washed sequentially with water and brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216968B2
Source datasetuspto-grants-2015_12
ORD IDord-ea7a4f8b9a3943109dd6176537cc9524
Source noteuspto-grants-2015_12