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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1484451생성일: 2026년 10월 26일

6-Chloroimidazo[2,1-b][1,3]thiazole-5-sulfonamide → HCID 178485216, 화합물

https://huagongshe.com/reaction/1484451

반응식

참여 물질

역할이름HCID투입량
반응물6-Chloroimidazo[2,1-b][1,3]thiazole-5-sulfonamideHCID 2779839—
반응물N-methyl-8-oxa-2,3-diaza-spiro[4.5]dec-3-ene-2-carboximidothioic acid methyl esterHCID 67360788—
용매AcetonitrileHCID 6342—
생성물HCID 178485216HCID 17848521669%

반응 단계

0.42 g (1 mol equiv.) N-Methyl-8-oxa-2,3-diaza-spiro[4.5]dec-3-ene-2-carboximidothioic acid methyl ester and 0.46 g (1.05 mol equiv.) 6-chloro-imidazo[2,1-b]thiazole-5-sulfonic acid amide were added to 7 mL acetonitrile and the reaction mixture was refluxed overnight. Volatiles were removed under reduced pressure, and the residue was taken up in ethylacetate and extracted with 2N NaOH. The organic layer was dried over Na2SO4, filtered and evaporated to dryness. Purification by flash chromatography on silica gel (EtOAc) afforded 0.56 g (69%) 6-chloro-imidazo[2,1-b]thiazole-5-sulfonic acid methylamino-(8-oxa-2,3-diaza-spiro[4.5]dec-3-en-2-yl)-methylene-amide. 1H NMR (400 MHz, CDCl3) δ 1.51-1.57 (m, 2H), 1.80-1.89 (m, 2H), 3.10 (d, J=5.0 Hz, 3H), 3.51-3.59 (m, 2H), 3.83-3.90 (m, 4H), 3.89 (s, 2H), 6.89 (s, 1H), 6.99 (d, J=4.6 Hz, 1H), 7.12 (br.s., 1H), 8.01 (d, J=4.6 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09422244B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-efd19343a54c46ca985cd9c28e61078d
출처 메모uspto-grants-2016_08