Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → 4-((4-Oxo-2-thioxothiazolidin-3-yl)methyl)benzenesulfonamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Mafenide Hydrochloride | HCID 67313 | — |
| 반응물 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 반응물 | 3,5-Dithia-4-thioxo-1,7-heptanedioic acid | HCID 80618 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-((4-Oxo-2-thioxothiazolidin-3-yl)methyl)benzenesulfonamide | HCID 33679359 | 70.7% |
반응 단계
To a solution of bis(carboxymethyl)trithiocarbonate (200 mg) in tetrahydrofuran (10 ml) was added carbonyldiimidazole (291 mg), and the mixture was stirred at room temperature. After 2 hr, to the reaction mixture were added homosulfamine hydrochloride (200 mg) and N,N-diisopropylethylamine (155 mg), and the mixture was stirred overnight at 70° C. 2N Hydrochloric acid (10 ml) was added thereto under ice cooling, the mixture was extracted twice with ethyl acetate (40 ml), and the extract was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=2:1) to give 3-(4-sulfamoylbenzyl)-2-thioxothiazolidin-4-one (189 mg).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09056862B2 |
| 출처 데이터셋 | uspto-grants-2015_06 |
| ORD ID | ord-67e3bd37cd1e4a92ac033706125b7538 |
| 출처 메모 | uspto-grants-2015_06 |