Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Morpholine → 3-(Morpholinosulfonyl)pyridine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Morpholine | HCID 8083 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Phosphorus pentachloride | HCID 24819 | — |
| 반응물 | 3-Pyridinesulfonic acid | HCID 69468 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | Pyridine-3-sulfonyl chloride | HCID 3164136 | — |
| 생성물 | 3-(Morpholinosulfonyl)pyridine | HCID 4276436 | 81% |
반응 단계
Pyridine-3-sulfonyl chloride was prepared from phosphorus pentachloride (17.82 g, 0.112 mol) and pyridine-3-sulfonic acid (12.36 g, 77.7 mmol) according to the procedure described by P. Breant et al. Synthesis, 1983, 822. Anhydrous toluene (20 mL) was added to the product and this solution added slowly to a mixture of toluene (100 mL), triethylamine (4 eq, 43 mL) and morpholine (1.5 eq, 10.3 mL) with cooling in ice water. A thick precipitate was formed. The mixture was stirred for 16 hr and then shaken with a saturated K2CO3 solution, dried over anhydrous sodium sulfate and evaporated to give a yellowish brown solid. Trituration with methanol gave 4-(pyridine-3-sulfonyl)-morpholine as a pale yellow solid (14.29 g, 81%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06979741B2 |
| 출처 데이터셋 | uspto-grants-2005_12 |
| ORD ID | ord-bc41d7d1737f4fca93c428f6248810d9 |
| 출처 메모 | uspto-grants-2005_12 |