돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 560550생성일: 2026년 10월 24일

N-Benzylethylenediamine → 2-Benzyl-1,2,5-thiadiazolidine 1,1-dioxide

https://huagongshe.com/ko/reaction/560550

반응식

참여 물질

역할이름HCID투입량
반응물N-BenzylethylenediamineHCID 77801—
반응물SulfamideHCID 82267—
용매PyridineHCID 1049—
생성물2-Benzyl-1,2,5-thiadiazolidine 1,1-dioxideHCID 1037589040%

반응 단계

To a solution of N-benzylethane-1,2-diamine (1.00 g, 6.65 mmol) in pyridine (10 mL) was added sulfamide (0.77 g, 7.98 mmol). The mixture was refluxed for 16 hours. The solvent was removed in vacuo. The residue was diluted with ethyl acetate (100 mL), washed with water (200 mL) and brine (100 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography eluted with ethyl acetate/hexane (1/4) to afford the title compound as an oily solid in 40% yield (0.57 g): 1H NMR (300 MHz, CDCl3) δ 7.35-7.27 (m, 5H), 4.59 (br s, 1H), 4.15 (s, 2H), 3.48-3.42 (m, 2H), 3.27-3.22 (m, 2H); MS (ES+) m/z 213.2 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063084B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-e14c6f0b0c3943e1a443ce0b6e6e5565
출처 메모uspto-grants-2011_11