Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → 2-(N-methanesulfonyl-4-piperidinyloxy)-5-chloropyridine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | 5-Chloro-2-(piperidin-4-yloxy)pyridine | HCID 11264329 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-(N-methanesulfonyl-4-piperidinyloxy)-5-chloropyridine | HCID 22719719 | 86.6% |
반응 단계
To a solution 2-(4-piperidinyloxy)-5-chloropyridine(12.9 g, 0.06 mol) and Et3N (25.4 ml, 0.182 mol) in dry dichloromethane (400 ml) at 0° C. and under Argon, was added methanesulfonyl chloride (5.3 ml, 0.067 mol) in dry dichloromethane (100 ml), dropwise. The mixture was stirred for 20 hours at room temperature. The mixture was diluted with dichloromethane (250 ml), then washed with water (×3) then brine. The organic layers were dried with Na2SO4 and evaporated in vacuo. The residue was triturated and washed with diethylether to give 2-(N-methanesulfonyl-4-piperidinyloxy)-5-chloropyridine (15.1 g) as a pale yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06734184B1 |
| 출처 데이터셋 | uspto-grants-2004_05 |
| ORD ID | ord-97ee7243a24d4f11b155705a57c6c212 |
| 출처 메모 | uspto-grants-2004_05 |