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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1603190생성일: 2026년 10월 27일

Hydrochloric Acid → N-(p-azidobenzenesulfonyl) N'-(3-carboxypropionyl) cystamine

https://huagongshe.com/reaction/1603190

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Cystamine DihydrochlorideHCID 5941—
반응물Succinic anhydrideHCID 7922—
반응물Sodium HydroxideHCID 14798—
반응물N-(p-azidobenzenesulfonyl)-N'-(3-succinimidyloxycarbonyl-propionyl)cystamineHCID 19609028—
용매WaterHCID 962—
생성물N-(p-azidobenzenesulfonyl) N'-(3-carboxypropionyl) cystamineHCID 19609019—

반응 단계

2.2 g of cystamine dihydrochloride were dissolved in 20 ml of water and adjusted to pH 10 with NaOH. 2.1 g of p-azidobenzenesulfochloride were suspended in the solution and the mixture was stirred at room temperature for 5 hours. The precipitated N-(p-azidobenzenesulfonyl)cystamine was reacted with 2 g of succinic anhydride and stirred overnight. The resulting solution was acidified with HCl and the product was subsequently filtered off and washed with water. The residue was dried at room temperature in a high vacuum and gave 1.53 g of N-(p-azidobenzenesulfonyl)-N'-(3-carboxypropionyl)cystamine. The IR showed bands at 3283 (amide NH), 2134 (azide), 1714 (acid carbonyl), 1650 (amide), 1589+1547 (aromatic), 1284 (COOH), 1328+1180 (arylsulfonyl), 839 (p- disubst. benzene); TLC (silica gel: conc. NH3 (EtOH=1%). Rf=0.7; m.p. 163° (dec.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05986066
출처 데이터셋uspto-grants-1999_11
ORD IDord-1098af0e084b48738a80de62db0fe224
출처 메모uspto-grants-1999_11