Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 61946생성일: 2026년 10월 25일
Isopropylamine → 3-bromo-N-[4-chloro-2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide
https://huagongshe.com/reaction/61946
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Isopropylamine | HCID 6363 | — |
| 반응물 | 2-(3-Bromo-1-(3-chloropyridin-2-yl)-1H-pyrazol-5-yl)-6-chloro-8-methyl-4H-benzo[d][1,3]oxazin-4-one | HCID 10253307 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-bromo-N-[4-chloro-2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide | HCID 11663488 | — |
반응 단계
To a solution of 2-[3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazol-5-yl]-6-chloro-8-methyl-4H-3,1-benzoxazin-4-one (i.e. the benzoxazinone product of Step E) (0.20 g, 0.44 mmol) in tetrahydrofuran was added isopropylamine (0.122 mL, 1.42 mmol), and the reaction mixture was heated to 60° C. for 90 minutes and then cooled to room temperature. The tetrahydrofuran solvent was evaporated under reduced pressure, and the residual solid was triturated with ether, filtered, and dried to afford the title compound, a compound of the present invention, as a solid (150 mg), m.p. 159-161° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09445593B1 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-030628cda8124ca6ba71e9b5a6bd09e0 |
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| 출처 메모 | uspto-grants-2016_09 |
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