참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyridine-2-carbonitrile | HCID 7522 | — |
| 반응물 | 4-(Methylsulfonyl)aniline hydrochloride | HCID 2735180 | — |
| 반응물 | Trimethylaluminum | HCID 16682925 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | HCID 178504797 | HCID 178504797 | — |
반응 단계
To a suspension of 4-(methylsulfonyl)aniline hydrochloride (6 g, 28.8 mmol) in toluene (150 ml) at 0° C., trimethylaluminum (2M solution in toluene, 21.6 ml, 43.2 mmol) was added over 15 minutes. The reaction mixture was warmed to room temperature and stirred for 2.5 hours. A solution of 2-cyanopyridine (6 g, 57.6 mmol) in toluene (150 ml) was added over 10 minutes and the reaction mixture was heated to 85°-90° C. After 24 hours, the reaction mixture was cooled to room temperature and poured over a slurry of silica gel in chloroform. After filtration, the residue was washed with a mixture of methylene chloride/methanol and later methanol. The combined filtrates were concentrated and the resulting yellowish solid was stirred with ethyl acetate (1500 ml) and filtered. The pale yellow solid (5.2 g, 66%) was used in the next reaction without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US05616601 |
|---|
| 출처 데이터셋 | uspto-grants-1997_04 |
|---|
| ORD ID | ord-5222de9267fa43ebad89cdeb17a5147f |
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| 출처 메모 | uspto-grants-1997_04 |
|---|