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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 583482생성일: 2026년 10월 25일

N-Trimethylsilyl-N-methylacetamide → N-[(4-sulfamoylphenyl)methyl]-2-[[2-[(4-sulfamoylphenyl)methylcarbamoyl]phenyl]disulfanyl]benzamide

https://huagongshe.com/reaction/583482

반응식

참여 물질

역할이름HCID투입량
반응물N-Trimethylsilyl-N-methylacetamideHCID 81953—
반응물2,2'-Dithiodibenzoyl chlorideHCID 88164—
반응물4-(Aminomethyl)benzenesulfonamide hydrochloride hydrateHCID 21584567—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물N-[(4-sulfamoylphenyl)methyl]-2-[[2-[(4-sulfamoylphenyl)methylcarbamoyl]phenyl]disulfanyl]benzamideHCID 46536935.4%

반응 단계

A slurry of 4-(aminomethyl)benzenesulfonamide hydrochloride hydrate (6.5 gf 29 mmol) in 100 mL pyridine was allowed to stir with N-methyl-N-(trimethylsilyl)acetamide (13.4 mL, 83.0 mmol) until a homogenous solution occurred. The solution was cooled to 0° C. to 5° C. and a solution of 2,2'-dithiobisbenzoyl chloride (4.0 g, 16.0 mmol) in 20 mL dichloromethane was added dropwise. The resulting solution was allowed to stir for 18 hours and the dichloromethane was removed in vacuo. The crude product was precipitated with the addition of water and the resulting solid was collected by filtration. The crude product was recrystallized from a mixture of dimethylformamide, ethanol, and water to yield 3.3 g of the title compound, mp 267-269° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05929114
출처 데이터셋uspto-grants-1999_07
ORD IDord-5aad2cea920c49739b25da5c2dc544c4
출처 메모uspto-grants-1999_07