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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007726Generated: October 31, 2026

Thionyl Chloride → HCID 22669217, compound

https://huagongshe.com/reaction/1007726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant1-Cyclohexyl-2-(furan-3-yl)-1H-benzimidazole-5-carboxylic acidHCID 491113—
SolventDimethylformamideHCID 6228—
ProductHCID 22669217HCID 22669217—

Reaction Steps

The carboxylic acid of example 2 (0.550 g, 1.8 mmol) was dissolved in SOCl2 (20 mL) and DMF (˜0.1 mL). The reaction mixture was stirred at room temperature for 20 h and then concentrated to dryness and co-evaporate with EtOAc to give a 1-cyclohexyl-2-furan-3-yl-1H-benzoimidazole-5-carbonyl chloride as a brown solid (580 mg). The acid chloride (0.050 g, 0.16 mmol) was dissolved in DMF (1 mL) and reacted with 1-carnosine (0.036 g, 0.159 mmol) in the presence of DIEA (82 μL, 0.476 mmol). The reaction mixture was stirred for 3 days at room temperature before it was acidified with AcOH (1 mL) and purified by reversed phase C18 preparative HPLC. The title compound of example 145 was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794404B2
Source datasetuspto-grants-2004_09
ORD IDord-9b5e28588a8b4d4ca1fe8cd096c9024f
Source noteuspto-grants-2004_09