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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1616037생성일: 2026년 10월 25일

Diisopropylethylamine → 5-Amino-N-[6-(1H-indol-4-yl)-1H-indazol-4-yl]-2-pyridinecarboxamide

https://huagongshe.com/reaction/1616037

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물5-Aminopyridine-2-carboxylic acidHCID 4179726—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물6-(1H-indol-4-yl)-1H-indazol-4-amineHCID 58268019—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
용매Dimethyl sulfoxide methanolHCID 22036561—
생성물5-Amino-N-[6-(1H-indol-4-yl)-1H-indazol-4-yl]-2-pyridinecarboxamideHCID 4453983238%

반응 단계

To a solution of 5-amino-2-pyridinecarboxylic acid (56 mg, 0.40 mmol, available from ChemPacific) in DMF (2 ml) was added HATU (150 mg, 0.40 mmol) and DIPEA (0.211 ml, 1.21 mmol). The mixture was stirred at room temperature for 20 mins then 6-(1H-indol-4-yl)-1H-indazol-4-amine (50 mg, 0.20 mmol) was added and the mixture stirred at room temperature for 18 h. The reaction mixture was added to the top of a 20 g aminopropyl cartridge that had been preconditioned with MeOH. The reaction mixture remained on the cartridges for 3 h before being eluted with MeOH. The solvent was removed in vacuo to give a crude residue that was dissolved in DMSO/MeOH (1:1) and purified by Mass Directed Automated Preparative HPLC (Method C). The product was loaded onto a 1 g aminopropyl column, eluted with DCM/MeOH (1:1) and the solvent removed under a stream of nitrogen to give the title compound (28 mg) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08765743B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-57383f8ef4e04e1bba4899aee3374b40
출처 메모uspto-grants-2014_07