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HRID 1515295생성일: 2026년 10월 26일

Sodium methanesulfonate → {5-Chloro-2-[(R)-4-(2-methanesulfonyl-ethyl)-4,5-dihydro-thiazol-2-yl]-1H-indol-7-yl}-cyclopentyl-amine

https://huagongshe.com/reaction/1515295

반응식

참여 물질

역할이름HCID투입량
반응물Sodium methanesulfonateHCID 638112—
반응물2-[(R)-2-(5-chloro-7-cyclopentylamino-1H-indol-2-yl)-4,5-dihydro-thiazol-4-yl]-ethanolHCID 25196146—
용매DimethylformamideHCID 6228—
생성물{5-Chloro-2-[(R)-4-(2-methanesulfonyl-ethyl)-4,5-dihydro-thiazol-2-yl]-1H-indol-7-yl}-cyclopentyl-amineHCID 5954307645%

반응 단계

2-[(R)-2-(5-chloro-7-cyclopentylamino-1H-indol-2-yl)-4,5-dihydro-thiazol-4-yl]-ethanol (50 mg, 0.11 mmol) prepared in Example 5 was dissolved in N,N-dimethylformamide (2 mL). Sodium methanesulfonate (54 mg, 0.55 mmol) was added thereto, and the mixture was stirred for 8 h at room temperature. The reaction was quenched by water. The reaction mixture was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (19 mg, Yield 45%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08222414B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-e0e2d79909af47028fee685e7a4decbd
출처 메모uspto-grants-2012_07