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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1045890생성일: 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/1045890

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 번호US08569307B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-7035704a0fcc495d85c175797c3d9442
출처 메모uspto-grants-2013_10