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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850358Generated: October 30, 2026

Sodium Carbonate → HCID 58547178, compound

https://huagongshe.com/reaction/1850358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
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 67469212HCID 67469212—
SolventDichloromethaneHCID 6344—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductHCID 58547178HCID 5854717827%

Reaction Steps

The mixture of 2-azetidin-3-yl-3-(2-methoxy-phenoxy)-pyrazine hydrochloride (108 mg, 0.37 mmol), HATU (280 mg, 0.74 mmol) and TEA (130 mg, 1.3 mmol) in dry DCM (10 mL) was stirred at RT for 30 min, then 1H-benzoimidazole-2-carboxylic acid was added to the solution. The solution was heated to 80° C. overnight. The mixture was poured into saturated aqueous Na2CO3 and extracted with DCM (50 mL×2). The organic layer was washed with brine, dried over Na2SO4 and concentrated to give the crude compound, which was purified by ISCO silica gel column (10% to 80% EtOAc in petroleum ether) and followed by reverse phase prep. HPLC (10% to 80% water/MeCN) to give (1H-benzoimidazol-2-yl)-{3-[3-(2-methoxy-phenoxy)-pyrazin-2-yl]-azetidin-1-yl}-methanone (40 mg, 0.11 mmol, yield 27%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957073B2
Source datasetuspto-grants-2015_02
ORD IDord-58c85570a15a4b49ab5e74eabce18bb9
Source noteuspto-grants-2015_02