돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 341441생성일: 2026년 10월 26일

Triphenyl(3,3,3-trifluoropropyl)phosphanium iodide → 2-N-Methyl-2-N-phenyl-6-{5-[4-(3,3,3-trifluoropropylidene)piperidin-1-yl]-1,2,4-oxadiazol-3-yl}-1,3,5-triazine-2,4-diamine

https://huagongshe.com/reaction/341441

반응식

참여 물질

역할이름HCID투입량
반응물Triphenyl(3,3,3-trifluoropropyl)phosphanium iodideHCID 19694095—
반응물Potassium tert-butoxideHCID 23665647—
반응물1-(3-{4-Amino-6-[methyl(phenyl)amino]-1,3,5-triazin-2-yl}-1,2,4-oxadiazol-5-yl)piperidin-4-oneHCID 66803163—
용매DichloromethaneHCID 6344—
용매1,4-DioxaneHCID 31275—
생성물2-N-Methyl-2-N-phenyl-6-{5-[4-(3,3,3-trifluoropropylidene)piperidin-1-yl]-1,2,4-oxadiazol-3-yl}-1,3,5-triazine-2,4-diamineHCID 6680270512%

반응 단계

To a solution of triphenyl-(3,3,3-trifluoro-propyl)-phosphonium iodide (146 mg, 0.30 mmol) in anhydrous dioxane (10 mL) at 0 C under nitrogen was added potassium tert-butoxide (34 mg, 0.3 mmol) portion-wise. The suspension was stirred for 10 min at 0 C and then added drop-wise to a solution of 1-{3-[4-amino-6-(methyl-phenyl-amino)-[1,3,5]triazin-2-yl]-[1,2,4]oxadiazol-5-yl}-piperidin-4-one (Intermediate 131, 55 mg, 0.150 mmol) in anhydrous dioxane (10 mL). The resulting reaction mixture was stirred at room temperature for 16 h and evaporated to dryness. The solid obtained was dissolved in DCM (25 mL) and washed with water (25 mL), a saturated ammonium chloride aq. solution (25 mL) and brine (25 mL). The organic phase was dried over magnesium sulfate, evaporated to dryness and purified by preparative HPLC-MS (Method B) to afford the title compound as an off-white solid (8 mg, 12%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895733B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-5089c52427c043a3bfcd23c7bf57d7b5
출처 메모uspto-grants-2014_11