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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1510811생성일: 2026년 10월 26일

Water → N-(2-Chloro-4-methylpyridin-3-yl)-2-(cyclopropylamino)nicotinamide

https://huagongshe.com/reaction/1510811

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물CyclopropylamineHCID 69828—
반응물Potassium FluorideHCID 522689—
반응물2-Chloro-N-(2-chloro-4-methyl-3-pyridinyl)-3-pyridinecarboxamideHCID 10423868—
용매O-XyleneHCID 7237—
생성물N-(2-Chloro-4-methylpyridin-3-yl)-2-(cyclopropylamino)nicotinamideHCID 9972204—

반응 조건

온도135 °C

반응 단계

2-Chloro-N-(2-chloro-4-methyl-3-pyridinyl)-3-pyridine carboxamide (100 g), potassium fluoride (22.62 g), cyclopropylamine (80.85 g) were suspended in o-xylene (300 ml) and heated to 130-140° C. in autoclave for 5-9 h. Then the reaction mass was cooled to 25-30° C., diluted with o-xylene (500 ml) and further heated the reaction mass to 70-75° C. Thereafter, DM water (300 ml) added and stirred for 10 min at 70-75° C. The aqueous layer was separated at hot condition and organic layer was washed with DM water (300 ml) at 70-75° C. and organic layer was concentrated at 60-63° C. under reduced pressure up to residue weight attained is approximately 400 g. The concentrated mass was cooled to 25-30° C. and stirred for 15 min and further cooled to 5-10° C. and stirred for 30 min. Filtered the solid obtained and washed with chilled o-xylene (100 ml, 5-10° C.). Dried the obtained solid at 50-60° C. under reduced pressure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08212025B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-f0479f02c46f43e5a248a3daa2e0b0d5
출처 메모uspto-grants-2012_07