Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methanesulfinyl chloride → Methanesulfinic acid (6-chloro-pyridin-3-yl methyl)-amide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methanesulfinyl chloride | HCID 548463 | — |
| 반응물 | 5-(Aminomethyl)-2-chloropyridine | HCID 7020927 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Methanesulfinic acid (6-chloro-pyridin-3-yl methyl)-amide | HCID 58545437 | — |
반응 단계
Methanesulfinyl chloride was obtained as described in the literature. A solution of C-(6-chloro-pyridin-3-yl)-methylamine (2.1) (25 g, 178 mmol) in tetrahydrofuran (200 ml) was cooled to 0° C. and methanesulfinyl chloride (7 g, 71 mmol) was added dropwise. The solution was allowed to warm to room temperature and stirred for 16 hours. The precipitate was removed by filtration, the filtrate was diluted with EtOAc and washed with H2O. The organic phase was dried over Na2SO4 and evaporated under reduced pressure.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08252939B2 |
| 출처 데이터셋 | uspto-grants-2012_08 |
| ORD ID | ord-3be19a7127c34e83a55bdf5cf018e576 |
| 출처 메모 | uspto-grants-2012_08 |