Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 62317생성일: 2026년 10월 24일
1,2-Dichloroethane → N-((4,6-Dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-1-isopropyl-6-(trifluoromethyl)-1H-indole-4-carboxamide
https://huagongshe.com/ko/reaction/62317
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1,2-Dichloroethane | HCID 11 | — |
| 반응물 | 4-Methylmorpholine | HCID 7972 | — |
| 반응물 | HOAt | HCID 181649 | — |
| 반응물 | 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridin-2-one | HCID 7063844 | — |
| 반응물 | 1-Isopropyl-6-(trifluoromethyl)-1H-indole-4-carboxylic acid | HCID 67464224 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 생성물 | N-((4,6-Dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-1-isopropyl-6-(trifluoromethyl)-1H-indole-4-carboxamide | HCID 67468150 | 65.4% |
반응 단계
To a solution of 1-(1-methylethyl)-6-(trifluoromethyl)-1H-indole-4-carboxylic acid (40 mg, 0.147 mmol) in dimethyl sulfoxide (1 mL) were added 3-(aminomethyl)-4,6-dimethyl-2(1H)-pyridinone (41.7 mg, 0.221 mmol), N-methylmorpholine (0.065 mL, 0.590 mmol), 1-hydroxy-7-azabenzotriazole (40.1 mg, 0.295 mmol) and EDC (56.5 mg, 0.295 mmol), and the mixture was stirred overnight. The mixture was quenched with water (5 mL) and stirred for 10 min. The precipitate was collected by filtration and dried under high vacuum to give the title compound (39 mg, 63%) as an off-white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.47 (m, 6H), 2.13 (s, 3H), 2.23 (s, 3H), 4.36 (d, J=5.05 Hz, 2H), 4.99 (dt, J=13.20, 6.66 Hz, 1H), 5.89 (s, 1H), 6.98 (d, J=3.03 Hz, 1H), 7.68 (s, 1H), 7.86 (d, J=3.28 Hz, 1H), 8.08 (s, 1H), 8.45 (t, J=4.93 Hz, 1H), 11.56 (s, 1H). MS: (M+H)+=406.1.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09446041B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-e49beb8c51ea4fe2bfb63a768d9fd1cc |
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| 출처 메모 | uspto-grants-2016_09 |
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