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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1671666생성일: 2026년 10월 26일

Dimethylamine → 3,4-Dimethoxy-N-[4-(3-nitrophenyl)-5-dimethylaminomethyl-1,3-thiazole-2-yl]benzenesulfonamide

https://huagongshe.com/reaction/1671666

반응식

참여 물질

역할이름HCID투입량
반응물DimethylamineHCID 674—
반응물FormaldehydeHCID 712—
반응물WaterHCID 962—
반응물3,4-Dimethoxy-N-(4-(3-nitrophenyl)-2-thiazolyl)benzenesulfonamideHCID 5282337—
용매EthanolHCID 702—
생성물3,4-Dimethoxy-N-[4-(3-nitrophenyl)-5-dimethylaminomethyl-1,3-thiazole-2-yl]benzenesulfonamideHCID 2481212486.3%

반응 단계

To a stirred solution of 3,4-dimethoxy-N-(4-(3-nitrophenyl)thiazol-2-yl)benzenesulfonamide (0.267 g, 0.68 mmol) in ethanol (10 mL, warming required) was added an aqueous solution of formaldehyde (37%, 0.5 mL, about 0.194 g, 6.5 mmol) followed by the dropwise addition of a solution of dimethylamine in water (60 wt %, 55 mL, about 0.274 g, 6.1 mmol). The addition was slightly exothermic, and the pale yellow solution became yellow-orange in color. After 0.5 h, a pale yellow solid separated from solution. After 19 h, the solid was collected by filtration, it was washed with ethanol, and dried in vacuo to give a pale yellow solid (0.277 g, 86.3% yield), mp 203° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07994338B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-b76905cfb3204e5985abab8a11309238
출처 메모uspto-grants-2011_08