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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 85484생성일: 2026년 10월 24일

3-(Aminomethyl)-6-methyl-4-propylpyridin-2(1H)-oneacetate → 6-bromo-1-isopropyl-3-methyl-N-((6-methyl-2-oxo-4-propyl-1,2-dihydropyridin-3-yl)methyl)-1H-indazole-4-carboxamide

https://huagongshe.com/ko/reaction/85484

반응식

참여 물질

역할이름HCID투입량
반응물3-(Aminomethyl)-6-methyl-4-propylpyridin-2(1H)-oneacetateHCID 67124140—
반응물6-bromo-1-isopropyl-3-methyl-1H-indazole-4-carboxylic acidHCID 67467127—
생성물6-bromo-1-isopropyl-3-methyl-N-((6-methyl-2-oxo-4-propyl-1,2-dihydropyridin-3-yl)methyl)-1H-indazole-4-carboxamideHCID 54596223—

반응 단계

The title compound was prepared in the same manner as described for example 3 (step c) from 6-bromo-3-methyl-1-(1-methylethyl)-1H-indazole-4-carboxylic acid (0.24 g, 0.808 mmol) and 3-(aminomethyl)-6-methyl-4-propyl-2(1H)-pyridinone (0.219 g, 1.010 mmol). The title compound was collected as a white solid (0.35 g, 92%); 1H NMR (400 MHz, DMSO-d6) δ ppm 0.92 (t, J=7.33 Hz, 3H) 1.41 (d, J=6.57 Hz, 6H) 1.49-1.60 (m, 2H) 2.12 (s, 3H) 2.39 (s, 3H) 2.53 (s, 1H) 4.33 (d, J=5.05 Hz, 2H) 4.88-5.00 (m, 1H) 5.89 (s, 1H) 7.12 (d, J=1.52 Hz, 1H) 8.02 (d, J=1.77 Hz, 1H) 8.48 (t, J=4.93 Hz, 1H) 11.50 (s, 1H); LCMS (ES+): 459.1 [M+H].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846935B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-3fef6be4ac8a4ca8bc96838fcb3fe886
출처 메모uspto-grants-2014_09