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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 327174생성일: 2026년 10월 24일

p-Nitrophenyl-2-aminothiazol-5-ylsulphone → 5-[(4-Nitrophenyl)sulfonyl]thiazole

https://huagongshe.com/ko/reaction/327174

반응식

참여 물질

역할이름HCID투입량
반응물p-Nitrophenyl-2-aminothiazol-5-ylsulphoneHCID 1535—
반응물Ammonium HydroxideHCID 14923—
반응물Hypophosphoric acidHCID 24536—
반응물Sodium NitriteHCID 23668193—
용매WaterHCID 962—
용매Phosphoric AcidHCID 1004—
생성물5-[(4-Nitrophenyl)sulfonyl]thiazoleHCID 1070715335.2%

반응 조건

온도-5 °C

반응 단계

To a cooled (-5° C.), stirred solution of 2-amino-5-[(4-nitrophenyl)sulfonyl]thiazole (5.15 g, 18.1 mmol) in 85% phosphoric acid (200 mL) was added dropwise a solution of sodium nitrite (1.56 g, 22.6 mmol) in distilled water (10 mL) at such a rate to maintain the internal temperature between -5° and 5° C. When the addition was complete the reaction mixture was stirred for 1 hour at 0° C. then treated dropwise with 50% hypophosphoric acid (15 mL). After the addition, the ice bath was removed and reaction mixture stirred at room temperature for 3 hours during which time moderate frothing occurred. The brown solution was diluted with water (total volume=1 L), neutralized with 28% ammonium hydroxide and filtered. Flash chromatography of the resulting brown solid (eluted with 5% v/v ethyl acetate in methylene chloride) yielded the title thiazole (1.72 g, 35%) as a yellow solid; mp 168°-170° C. 1H--NMR (250 MHz, d6 --DMSO): 8.32 (d, 2H, J=12.6 Hz, aromatic), 8.45 (d, 2H, J=12.8 Hz, aromatic), 8.74 (s, 1H, aromatic), 9.578 (s, 1H, aromatic). MS (CI, CH4): 271(M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05272163
출처 데이터셋uspto-grants-1993_12
ORD IDord-94ed8af1edb24399b0998ff8dde550fc
출처 메모uspto-grants-1993_12