Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetonitrile → 5-[3-(Benzenesulfonamido)propyloxy]imidazo[1,2-a]pyridine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | Benzenesulfonyl chloride | HCID 7369 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 5-[3-(Amino)propyloxy]imidazo[1,2-a]pyridine dihydrochloride | HCID 23362997 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 5-[3-(Benzenesulfonamido)propyloxy]imidazo[1,2-a]pyridine | HCID 23362978 | 59.5% |
반응 단계
To a suspension of 5-[3-(amino)propyloxy]imidazo[1,2-a]pyridine dihydrochloride (2.64 g, 10 mmoles) and triethylamine (4.88 ml, 35 mmoles) in methylene chloride (100 ml)-acetonitrile (30 ml) was added benzenesulfonyl chloride (1.53 ml, 12 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 1 hour. The reaction mixture was washed in turn with an aqueous sodium bicarbonate solution and saturated saline and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the crude product thus obtained was recrystallized from methylene-ethanol to obtain 1.97 g of the desired product (59.5%, light brown crystals).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05244908 |
| 출처 데이터셋 | uspto-grants-1993_09 |
| ORD ID | ord-87ae7e60b3f94aeab00f82581b06295a |
| 출처 메모 | uspto-grants-1993_09 |