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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

반응식

참여 물질

역할이름HCID투입량
반응물IsopropylamineHCID 6363—
반응물2-(3-Bromo-1-(3-chloropyridin-2-yl)-1H-pyrazol-5-yl)-6-chloro-8-methyl-4H-benzo[d][1,3]oxazin-4-oneHCID 10253307—
용매TetrahydrofuranHCID 8028—
생성물3-bromo-N-[4-chloro-2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamideHCID 11663488—

반응 조건

온도60 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09445593B1
출처 데이터셋uspto-grants-2016_09
ORD IDord-030628cda8124ca6ba71e9b5a6bd09e0
출처 메모uspto-grants-2016_09