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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850317Generated: October 31, 2026

2-Benzimidazolecarboxylic acid → HCID 54674275, compound

https://huagongshe.com/reaction/1850317

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Benzimidazolecarboxylic acidHCID 233240—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 67469208HCID 67469208—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 54674275HCID 5467427559%

Reaction Steps

To a mixture of 1H-benzoimidazole-2-carboxylic acid (124 mg, 0.76 mmol) in DMF (5 mL) was added TEA (152 mg, 1.5 mmol) and HATU (347 mg, 0.92 mmol). The reaction mixture was stirred for 5 min and 2-azetidin-3-yl-3-phenyl-pyridine hydrochloride (100 mg, 0.76 mmol) was added. The reaction mixture was stirred at RT overnight. The mixture was diluted with water (10 mL), and extracted with EtOAc (2×20 mL). The combined organic extracts were washed with water (5 mL) and brine (5 mL), dried over Na2SO4, and filtered. The filtrate was evaporated in vacuo and the residue was purified by column chromatography to give (1H-benzoimidazol-2-yl)-[3-(3-phenyl-pyridin-2-yl)-azetidin-1-yl]-methanone (100 mg, 0.28 mmol, 59% yield) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957073B2
Source datasetuspto-grants-2015_02
ORD IDord-56161959b638477eaa14879450c63537
Source noteuspto-grants-2015_02