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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 452545생성일: 2026년 10월 25일

Cesium carbonate → Formate

https://huagongshe.com/reaction/452545

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물Ethanamine, 2-chloro-N-methyl-, hydrochloride (1:1)HCID 3028223—
반응물HCID 178505857HCID 178505857—
용매AcetonitrileHCID 6342—
생성물FormateHCID 283—
생성물HCID 178484193HCID 178484193—

반응 조건

온도70 °C

반응 단계

A mixture of trans-8-chloro-1-[4-(3-fluoro-pyridin-2-yl)-cyclohexyl]-5,6-dihydro-4H-2,3,5,10b-tetraaza-benzo[e]azulene (50.0 mg, 0.126 mmol), cesium carbonate (246 mg, 0.754 mmol) and 2-methylaminoethyl chloride hydrochloride (65.4 mg, 0.503 mmol) in acetonitrile (1.3 ml) was heated at 70° C. for 20 h. After addition of further portions of cesium carbonate (246 mg, 0.754 mmol) and 2-methylaminoethyl chloride hydrochloride (65.4 mg, 0.503 mmol) the mixture was heated at 70° C. for another 20 h. The reaction mixture was partitioned between 1 M aqueous sodium hydroxide solution (2 ml) and ethyl acetate (5 ml). The layers were separated. The aqueous layer was extracted with two 5-ml portions of ethyl acetate. The combined organic layers were concentrated in vacuo. Preparative RP-HPLC with water (0.05% formic acid)/methanol as eluent gave the title compound as formate salt. The salt was partitioned between ethyl acetate (15 ml) and 1 M aqueous sodium hydroxide solution (10 ml). The layers were separated. The aqueous layer was extracted with two 15 ml-portions of ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and concentrated in vacuo to give the title compound (14 mg, 25%) as off-white solid. MS m/e: 455 ([M+H]+)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492376B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-2e4e64ee572a4846a88819af73d74256
출처 메모uspto-grants-2013_07