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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2172832생성일: 2026년 10월 26일

Hydrochloric Acid → 4-((4-Oxo-2-thioxothiazolidin-3-yl)methyl)benzenesulfonamide

https://huagongshe.com/reaction/2172832

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Mafenide HydrochlorideHCID 67313—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물3,5-Dithia-4-thioxo-1,7-heptanedioic acidHCID 80618—
반응물DiisopropylethylamineHCID 81531—
용매TetrahydrofuranHCID 8028—
생성물4-((4-Oxo-2-thioxothiazolidin-3-yl)methyl)benzenesulfonamideHCID 3367935970.7%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09056862B2
출처 데이터셋uspto-grants-2015_06
ORD IDord-67e3bd37cd1e4a92ac033706125b7538
출처 메모uspto-grants-2015_06