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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1750277생성일: 2026년 10월 26일

(S)-3-Methylpiperidine → 5-bromo-7-[(4-methylphenyl)sulfonyl]-4-[(3S)-3-methylpiperidin-1-yl]-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/1750277

반응식

참여 물질

역할이름HCID투입량
반응물(S)-3-MethylpiperidineHCID 641100—
반응물5-Bromo-4-Chloro-7-Tosyl-7H-Pyrrolo[2,3-D]PyrimidineHCID 57750282—
반응물3-{4-[(2S)-2-Methylmorpholin-4-yl]-7H-pyrrolo[2,3-d]pyrimidin-5-yl}benzonitrileHCID 72706904—
생성물5-bromo-7-[(4-methylphenyl)sulfonyl]-4-[(3S)-3-methylpiperidin-1-yl]-7H-pyrrolo[2,3-d]pyrimidineHCID 86706938—

반응 단계

5-Bromo-4-chloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidine (P3) was reacted with the hydrochloride salt of (3S)-3-methylpiperidine according to the method described for preparation of 3-{4-[(2S)-2-methylmorpholin-4-yl]-7H-pyrrolo[2,3-d]pyrimidin-5-yl}benzonitrile (6) in Example 6. In this case, purification was effected via silica gel chromatography (Eluent: 5:1 petroleum ether/ethyl acetate), providing the product as a white solid. Yield: 4.3 g, 9.6 mmol, 92%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09156845B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-fbe80560e72d44b58d74b7d688d41ba9
출처 메모uspto-grants-2015_10