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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40872생성일: 2026년 10월 24일

Diisopropylethylamine → 2-((R)-1-hydroxy-3-methylbutan-2-ylamino)-4-(5-methyl-1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidine-5-carbonitrile

https://huagongshe.com/ko/reaction/40872

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물D-ValinolHCID 6950587—
반응물4-(5-methyl-1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-2-(methylsulfonyl)pyrimidine-5-carbonitrileHCID 59414377—
용매TetrahydrofuranHCID 8028—
생성물2-((R)-1-hydroxy-3-methylbutan-2-ylamino)-4-(5-methyl-1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)pyrimidine-5-carbonitrileHCID 5941454777%

반응 단계

A mixture of 4-(5-methyl-1-tosyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-2-(methylsulfonyl)pyrimidine-5-carbonitrile (120 mg, 0.257 mmol), (R)-(−)-2-amino-3-methyl-1-butanol (57 μl, 0.515 mmol) and diisopropylethylamine (90 μl, 0.515 mmol) in THF (4 mL) was heated at reflux for 1 hour. The reaction mixture was concentrated in vacuo and the residue was purified on silica gel by flash column chromatography to give the title compound as a colourless glassy solid (97 mg, 77% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530489B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-7a32820803b64d7187b823db5dcd807c
출처 메모uspto-grants-2013_09