돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 448582생성일: 2026년 10월 25일

Sodium hydride → 4-[6-(5-Methanesulfonyl-2,3-dihydro-indol-1-yl)-pyrimidin-4-ylamino]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/448582

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물5-(Methanesulfonyl)-2,3-dihydro-1H-indoleHCID 2736136—
반응물tert-Butyl 4-[(6-chloropyrimidin-4-yl)amino]piperidine-1-carboxylateHCID 22309472—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물4-[6-(5-Methanesulfonyl-2,3-dihydro-indol-1-yl)-pyrimidin-4-ylamino]-piperidine-1-carboxylic acid tert-butyl esterHCID 5807412562.1%

반응 단계

To a solution of NaH (0.62 g, 15.5 mmol, 60% NaH) in 40 mL of DMF, 5-methanesulfonyl-2,3-dihydro-1H-indole (1.9 g, 9.63 mmol) was added and the mixture was stirred at room temperature for 30 minutes. 17a (3.09 g, 9.88 mmol) was added in DMF and the mixture was heated at 85° C. for 17 h. After cooling to room temperature, brine was added (200 mL) and the mixture was extracted with DCM (200 mL then 3×500 mL). The combined extracts were washed with brine (3×100 mL), dried, filtered and evaporated. The residue was purified by flash chromatography (eluent: 25 to 100% EtOAc in hexane with 0.1% triethylamine) to afford 2.83 g (62%) of 17b.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481731B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-193c47e56d1b44f9927c0f14fe6990bf
출처 메모uspto-grants-2013_07