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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30078생성일: 2026년 10월 25일

Water → 4-Chloro-6-((2,6-difluorophenyl)amino)-2-(methylthio)pyrimidine-5-carbaldehyde

https://huagongshe.com/reaction/30078

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물2,6-DifluoroanilineHCID 79647—
반응물4,6-Dichloro-2-(methylsulfanyl)pyrimidine-5-carbaldehydeHCID 4614004—
용매ChloroformHCID 6212—
생성물4-Chloro-6-((2,6-difluorophenyl)amino)-2-(methylthio)pyrimidine-5-carbaldehydeHCID 994473776.2%

반응 단계

To a solution of 4,6-dichloro-2-methylsulfanyl-pyrimidine-5-carbaldehyde (11.1 grams(hereinafter “g”), 50 millimoles (hereinafter “mmol”)) in CHCl3 (100 milliliters (hereinafter “mL”)) was added 2,6-difluoroaniline (8.07 mL, 75 mmol, 1.5 equivalents (hereinafter “eq”)) followed by Et3N (10.43 mL, 75 mmol, 1.5 eq). The reaction mixture turned yellow and was heated to reflux for 24 h, H2O (50 mL) was added and the layers were separated. The organic layer was evaporated and the crude product was recrystallized from 200 mL of a methanol: H2O mixture (2:1) to give 12.03 g (76%) of pure 4-chloro-6-(2,6-difluoro-phenylamino)-2-methylsulfanyl-pyrimidine-5-carbaldehyde. 1H-NMR: δ 2.21 (s, 3H), 6.91 (m, 2H), 7.24 (m, 1H), 10.29 (s, 1H), 10.35 (br s, 1H). LC MS (m/e)=316 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423042B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-5a62bd6a3fc94fc19220661b255ffe10
출처 메모uspto-grants-2008_09