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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 877554생성일: 2026년 10월 25일

3-Amino-1-propanol → 2-(6-chloro-4-(isopropylamino)pyridin-3-yl)-N-(3-hydroxypropyl)-5-methyloxazole-4-carboxamide

https://huagongshe.com/reaction/877554

반응식

참여 물질

역할이름HCID투입량
반응물3-Amino-1-propanolHCID 9086—
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물2-(6-Chloro-4-(isopropylamino)pyridin-3-yl)-5-methyloxazole-4-carboxylic acidHCID 89689747—
용매DimethylformamideHCID 6228—
생성물2-(6-chloro-4-(isopropylamino)pyridin-3-yl)-N-(3-hydroxypropyl)-5-methyloxazole-4-carboxamideHCID 89689652—

반응 단계

2-(6-chloro-4-(isopropylamino)pyridin-3-yl)-5-methyloxazole-4-carboxylic acid (30a) (100 mg, 0.338 mmol) was dissolved in DMF (5 mL). 3-aminopropan-1-ol (1.691 mmol, 5 equiv.) and DIPEA (1.353 mmol, 4 equiv.) were added to the reaction mixture and stirred at room temperature. HATU (1.014 mmol, 3 equiv.) was added to the reaction mixture and stirred for 3 h. The reaction mixture was concentrated under reduced pressure to remove excess of DMF. The residue obtained was partitioned between water and EtOAc. The organic layer was separated, dried over Na2SO4, filtered and concentrated. The crude material obtained was purified by flash column chromatography through silica gel and MeOH: CHCl3 as eluent to afford the title compound, 2-(6-chloro-4-(isopropylamino)pyridin-3-yl)-N-(3-hydroxypropyl)-5-methyloxazole-4-carboxamide (31).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08987311B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-0de7d337eb934649bfec00bb7d8b292f
출처 메모uspto-grants-2015_03