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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Amino-1-propanol | HCID 9086 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| 반응물 | 2-(6-Chloro-4-(isopropylamino)pyridin-3-yl)-5-methyloxazole-4-carboxylic acid | HCID 89689747 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-(6-chloro-4-(isopropylamino)pyridin-3-yl)-N-(3-hydroxypropyl)-5-methyloxazole-4-carboxamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08987311B2 |
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| 출처 데이터셋 | uspto-grants-2015_03 |
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| ORD ID | ord-0de7d337eb934649bfec00bb7d8b292f |
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| 출처 메모 | uspto-grants-2015_03 |
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