Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hexachloroethane → 6-Fluoro-3-isopropyl-[1,2,4]triazolo[4,3-a]pyridine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hexachloroethane | HCID 6214 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | Isobutyric acid N'-(5-fluoro-pyridin-2-yl)-hydrazide | HCID 66977821 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 6-Fluoro-3-isopropyl-[1,2,4]triazolo[4,3-a]pyridine | HCID 58783963 | — |
반응 단계
To a solution of Intermediate 1e (1.81 g, 9.18 mmol), triphenylphosphine (4.83 g, 18.4 mmol), and triethylamine (5.12 mL, 36.7 mmol) in THF (25 mL) at 0° C., hexachloroethane (4.36 g, 18.4 mmol) was added in 2 portions at a 1 min intervals. The resulting pale brown solution was allowed to warm to RT then stirred for 2 h. The resulting yellow suspension was filtered, washing with THF (2×25 mL). The combined organics were purified using SCX-2 cartridge (washed with DCM-MeOH (1:1, 100 mL) and MeOH (50 mL), and then the product was eluted with 2M NH3 in MeOH) to give a pale yellow solid (1.60 g, 97%, contaminated with ˜2.5% Ph3P═O). 1H NMR (400 MHz, CDCl3): 1.53 (6H, d), 3.32 (1H, sept), 7.15 (1H, ddd), 7.75 (1H, ddd), 7.84 (1H, m).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08835431B2 |
| 출처 데이터셋 | uspto-grants-2014_09 |
| ORD ID | ord-1af7344cea8a47188f6f1c9e0bb1b5db |
| 출처 메모 | uspto-grants-2014_09 |