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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850332Generated: October 30, 2026

Acetyl chloride → 1-(4-{3-[1-(1H-Benzoimidazole-2-carbonyl)-azetidin-3-YL]-pyrazin-2-YL}-3,6-dihydro-2H-pyridin-1-YL)-ethanone

https://huagongshe.com/reaction/1850332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant(1H-benzoimidazol-2-yl)-{3-[3-(1,2,3,6-tetrahydro-pyridin-4-yl)-pyrazin-2-yl]-azetidin-1-yl}-methanone hydrochlorideHCID 67469099—
SolventDichloromethaneHCID 6344—
Product1-(4-{3-[1-(1H-Benzoimidazole-2-carbonyl)-azetidin-3-YL]-pyrazin-2-YL}-3,6-dihydro-2H-pyridin-1-YL)-ethanoneHCID 5854685590%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (1H-benzoimidazol-2-yl)-{3-[3-(1,2,3,6-tetrahydro-pyridin-4-yl)-pyrazin-2-yl]-azetidin-1-yl}-methanone hydrochloride (187 mg, 0.47 mmol) in dry CH2Cl2 (10 mL) was added Et3N (1 mL). The reaction mixture was cooled to 0° C. with an ice bath, and acetyl chloride (39 mg, 0.50 mmol) was added dropwise. After 1 h, the reaction mixture was warmed to RT, and stirred overnight. Then the reaction mixture was washed with brine, dried over Na2SO4, filtered, and concentrated under vacuum to give the crude product (170 mg, 0.42 mmol, 90% yield). ESI-MS (M+1): 403 calc. for C22H22N6O2 402.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957073B2
Source datasetuspto-grants-2015_02
ORD IDord-f58417ab48144247b7e8df16fd5fc798
Source noteuspto-grants-2015_02