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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 440874생성일: 2026년 10월 25일

Sodium Hydroxide → (4-Pyridin-4-yl-pyrimidin-2-yl)-[3-(1,1,2,2-tetrafluoro-ethoxy)-phenyl]-amine

https://huagongshe.com/reaction/440874

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물2-Propen-1-one, 3-(dimethylamino)-1-(4-pyridinyl)-HCID 714531—
반응물3-(1,1,2,2-Tetrafluoroethoxy)phenylguanidine nitrateHCID 178512518—
용매IsobutanolHCID 6560—
생성물(4-Pyridin-4-yl-pyrimidin-2-yl)-[3-(1,1,2,2-tetrafluoro-ethoxy)-phenyl]-amineHCID 9799152—

반응 조건

온도110 °C

반응 단계

To a solution of 13.2 g (75 mmol) of 3-dimethylamino-1-(4-pyridyl)-2-propen-1-one [described in EP-A-0 233 461] in 500 ml of isobutanol are added 23.6 g (75 mmol) of 3-(1,1,2,2-tetrafluoroethoxy)phenylguanidine nitrate. Following the addition of 4 g (100 mmol) of sodium hydroxide, the reaction mixture is stirred for 3 hours at 110° C. The suspension is concentrated under reduced pressure, the residue is dissolved in 500 ml of methylene chloride/tetrahydrofuran (1:1), and the solution is extracted with 300 ml of water. The organic phase is dried over sodium sulfate and concentrated on a rotovap. Recrystallisation from diethyl ether/tetrahydrofuran gives N-[3-(1,1,2,2-tetrafluoroethoxy)phenyl]-4-(4-pyridyl)-2-pyrimidine-amine; Rf =0.9 (methylene chloride:methanol =9:1), FAB-MS: 365 (M+ +1), m.p. 191°-192°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05521184
출처 데이터셋uspto-grants-1996_05
ORD IDord-6d720e076e314b5c9a8896caa32adf55
출처 메모uspto-grants-1996_05