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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (1H-benzoimidazol-2-yl)-{3-[3-(1,2,3,6-tetrahydro-pyridin-4-yl)-pyrazin-2-yl]-azetidin-1-yl}-methanone hydrochloride | HCID 67469099 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-{3-[1-(1H-Benzoimidazole-2-carbonyl)-azetidin-3-YL]-pyrazin-2-YL}-3,6-dihydro-2H-pyridin-1-YL)-ethanone | HCID 58546855 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957073B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-f58417ab48144247b7e8df16fd5fc798 |
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| Source note | uspto-grants-2015_02 |
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