Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 551426생성일: 2026년 10월 26일
Carbonate Ion → 1-(4-fluorophenyl)-N-{[2-(trifluoromethyl)-2-oxiranyl]methyl}-indazol-4-amine
https://huagongshe.com/reaction/551426
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbonate Ion | HCID 19660 | — |
| 반응물 | Bismuth trichloride | HCID 24591 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | (2-(Trifluoromethyl)oxiran-2-yl)methyl 4-methylbenzenesulfonate | HCID 24809749 | — |
| 반응물 | 1-(4-Fluorophenyl)-1H-indazol-4-amine | HCID 24938058 | — |
| 촉매 | Bismuth trichloride | HCID 24591 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-(4-fluorophenyl)-N-{[2-(trifluoromethyl)-2-oxiranyl]methyl}-indazol-4-amine | HCID 24938056 | 59.1% |
반응 단계
[2-(trifluoromethyl)-2-oxiranyl]methyl 4-methylbenzenesulfonate (6.14 g, 20.75 mmol) and 1-(4-fluorophenyl)-1H-indazol-4-amine (4.73 g, 20.75 mmol) in dry dichloromethane (5 ml) were stirred for 5 min. Bismuth chloride (654 mg, 2.07 mmol) was added and the mixture stirred at room temperature over the weekend. More bismuth chloride (0.33 g, 1.05 mmol) was then added and the mixture stirred overnight. The reaction was finally stirred overnight under nitrogen (to reduce the volume of DMF). There was no further progress on leaving for a further night. The reaction mixture was then diluted with chloroform (200 ml) and tetrahydrofuran (50 ml). N,N-Diisopropylethylamine (0.54 ml, 3.11 mmol) was added followed by polymer supported carbonate resin (Fluka, ca. 3.5 mmoles carbonate/g resin, 11.91 g) and the mixture stirred overnight. More THF (30 ml) was then added followed after 2 hours by some 4 A molecular sieves. After a further 3 hours LCMS indicated the reaction to be complete and the mixture was filtered. The filtrate was washed with water, the aqueous phase was back-extracted with dichloromethane and the combined organic phases were dried and evaporated to give crude product which was purified by silica gel chromatography using the Flashmaster II (2×100 g cartridges) eluting with a 0 to 50% dichloromethane:ethyl acetate gradient to give the title compound (4.31 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07947727B2 |
|---|
| 출처 데이터셋 | uspto-grants-2011_05 |
|---|
| ORD ID | ord-b42ab2c801bc40188d392c1cf60a3bcb |
|---|
| 출처 메모 | uspto-grants-2011_05 |
|---|