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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 522120생성일: 2026년 10월 24일

Pyrazole, 4-amino-3,5-dimethyl- → 5-{[2,4-dichloro-5-(pyridin-2-yl)benzoyl]amino}-N-(3,5-dimethyl-1H-pyrazol-4-yl)-1-phenyl-1H-pyrazole-3-carboxamide

https://huagongshe.com/ko/reaction/522120

반응식

참여 물질

역할이름HCID투입량
반응물Pyrazole, 4-amino-3,5-dimethyl-HCID 78931—
반응물DiisopropylethylamineHCID 81531—
반응물5-(2,4-dichloro-5-(pyridin-2-yl)benzamido)-1-phenyl-1H-pyrazole-3-carboxylic acidHCID 118497035—
반응물HCID 178484293HCID 178484293—
용매DimethylformamideHCID 6228—
생성물5-{[2,4-dichloro-5-(pyridin-2-yl)benzoyl]amino}-N-(3,5-dimethyl-1H-pyrazol-4-yl)-1-phenyl-1H-pyrazole-3-carboxamideHCID 11849712549.6%

반응 단계

To a solution of 5-(2,4-dichloro-5-(pyridin-2-yl)benzamido)-1-phenyl-1H-pyrazole-3-carboxylic acid (Example 111, 110 mg, 0.24 mmol), 3,5-dimethyl-1H-pyrazol-4-amine (30 mg, 0.27 mmol) and DIPEA (0.17 mL, 0.97 mmol) in DMF (1.5 mL) was added 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate (101 mg, 0.26 mmol) and the reaction was stirred for 2 hours at room temperature. The reaction was concentrated in vacuo and the residue purified using Preparative HPLC to afford the title compound (65 mg, 49%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09328096B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-f765d43d60414545b93aa72d2a169944
출처 메모uspto-grants-2016_05