Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → N-(phenylsulfonyl)-benzo-1,2,3-thiadiazole-7-carboxylic acid amide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Benzenesulfonamide | HCID 7370 | — |
| 반응물 | 1,2,3-Benzothiadiazole-7-carbonyl chloride | HCID 18377607 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-(phenylsulfonyl)-benzo-1,2,3-thiadiazole-7-carboxylic acid amide | HCID 54415936 | — |
반응 단계
3.2 g of benzenesulfonamide are introduced at from 0°-5° C. into 50 ml of abs. pyridine and, while stirring at that temperature, a solution of 3.9 g of benzo-1,2,3-thiadiazole-7-carboxylic acid chloride in20 ml of methylene chloride is added dropwise. The mixture is stirred overnight and then poured onto ice-water, rendered slightly acidic with hydrochloric acid and extracted with methylene chloride, and the extracts are washed with water, dried and concentrated by evaporation. The residue is dissolved warm in tetrahydrofuran, treated with some silica gel, filtered, concentrated by evaporation and then recrystallised from tetrahydrofuran/hexane. The title compound resulting melts at 231°-233° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05051436 |
| 출처 데이터셋 | uspto-grants-1991_09 |
| ORD ID | ord-4fd4ff4754b84b008f3ee20d61297533 |
| 출처 메모 | uspto-grants-1991_09 |