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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505800Generated: October 31, 2026

Diisopropylethylamine → HCID 71267450, compound

https://huagongshe.com/reaction/1505800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantAzetidine hydrochlorideHCID 12308726—
ReactantHCID 71267437HCID 71267437—
SolventEthanolHCID 702—
ProductHCID 71267450HCID 7126745032.4%

Reaction Steps

A solution of 2-chloro-N-(3-chloro-2-methylphenyl)-6-({[2-(trifluoromethyl)phenyl]carbonyl}amino)-1H-benzimidazole-4-carboxamide (80 mg, Example 135), azetidine hydrochloride (60 mg) and N,N-diisopropylethylamine (208 μL) in EtOH (1.8 mL) was reacted at 120° C. for 20 minutes in a microwave reactor (Biotage, Initiator). The reaction mixture was concentrated under reduced pressure, and the residue was purified on column chromatography to obtain 2-(azetidin-1-yl)-N-(3-chloro-2-methylphenyl)-6-({[2-(trifluoromethyl)phenyl]carbonyl}amino)-1H-benzimidazole-4-carboxamide (27 mg). This was dissolved in MeOH (1 mL), 2N hydrogen chloride/MeOH solution (1 Eq) was added, and it was stirred and concentrated. The residue was triturated in diethyl ether, and the precipitate was collected by filtration and dried to obtain the titled compound (21 mg) as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216968B2
Source datasetuspto-grants-2015_12
ORD IDord-c3d87b1decac41a986bd123c33361205
Source noteuspto-grants-2015_12