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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Triphenyl(3,3,3-trifluoropropyl)phosphanium iodide | HCID 19694095 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 반응물 | 1-(3-{4-Amino-6-[methyl(phenyl)amino]-1,3,5-triazin-2-yl}-1,2,4-oxadiazol-5-yl)piperidin-4-one | HCID 66803163 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 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 | HCID 66802705 | 12% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08895733B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-5089c52427c043a3bfcd23c7bf57d7b5 |
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| 출처 메모 | uspto-grants-2014_11 |
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