Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 658492생성일: 2026년 10월 25일
1,1'-Carbonyldiimidazole → 4-[3-fluoro-4-({[(1-methyl-1H-indazol-5-yl)amino]carbonyl}amino)phenoxy]-N-methylpyridine-2-carboxamide
https://huagongshe.com/reaction/658492
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 반응물 | 1-methyl-1H-indazol-5-amine | HCID 2768032 | — |
| 반응물 | 4-(4-Amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide | HCID 46835219 | — |
| 용매 | Benzene | HCID 241 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-[3-fluoro-4-({[(1-methyl-1H-indazol-5-yl)amino]carbonyl}amino)phenoxy]-N-methylpyridine-2-carboxamide | HCID 10455583 | 27% |
반응 단계
To a solution of 1,1′-carbonyldiimidazole (62 mg, 0.38 mmol) in benzene (2 mL) and CH2Cl2 (1 mL) was added 4-(4-amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide (100 mg, 0.38 mmol). The resulting solution was stirred at room temperature for 16 h, then was treated with 1-methyl-5-aminoindazole (56 mg, 0.38 mmol). The reaction continued to stir at room temperature for 18 h. The mixture was concentrated under reduced pressure and the residue was triturated with Et2O. The solid was collected by filtration, and then purified by preparative HPLC to afford 44 mg (27%) of the title product. 1H-NMR (DMSO-d6) δ 2.78 (d, J=4.8, 3H), 4.01 (s, 3H), 7.02-7.07 (m, 1H), 7.14-7.18 (m, 1H), 7.28-7.36 (m, 2H), 7.39 (d, J=2.9, 1H), 7.52-7.59 (m, 1H), 7.89-7.96 (m, 2H), 8.23 (t, J=9.0, 1H), 8.49 (d, J=4.9, 1H), 8.57-8.63 (m, 1H), 8.71-8.81 (m, 1H), 9.06 (s, 1H); MS LC-MS [M+H]+=435.1; mp 231-234° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08076488B2 |
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| 출처 데이터셋 | uspto-grants-2011_12 |
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| ORD ID | ord-42cb988f1dd64c1da18e768779d9d0bc |
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| 출처 메모 | uspto-grants-2011_12 |
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