Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methane → 4-Amino-N-[4-(3-nitro-phenyl)-thiazol-2-yl]-benzenesulfonamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methane | HCID 297 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | N-{4-[4-(3-Nitro-phenyl)-thiazol-2-ylsulphamoyl]-phenyl}-acetamide | HCID 21845562 | — |
| 용매 | Hydrochloric Acid | HCID 313 | — |
| 생성물 | 4-Amino-N-[4-(3-nitro-phenyl)-thiazol-2-yl]-benzenesulfonamide | HCID 10407177 | 37.8% |
반응 단계
0.47 g of N-{4-[4-(3-nitro-phenyl)-thiazol-2-ylsulphamoyl]-phenyl}-acetamide was suspended in 10 ml of 6N hydrochloric acid and heated to boiling overnight. The cooled mixture was treated with 35 ml of 2N sodium hydroxide solution. After the addition of 0.4 g of active charcoal the mixture was stirred at room temperature for 30 minutes and subsequently the active charcoal was filtered off. The product separated upon neutralization with concentrated hydrochloric acid. Recrystallization from 50 ml of 40% ethanol yielded 0.16 g of 4-amino-N-[4-(3-nitro-phenyl)-thiazol-2-yl]-benzenesulfonamide as yellowish crystals.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05958910 |
| 출처 데이터셋 | uspto-grants-1999_09 |
| ORD ID | ord-eaf9c2605fe9486faf7aff7d5bd15277 |
| 출처 메모 | uspto-grants-1999_09 |