HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1484451Erstellt: 25. Oktober 2026
6-Chloroimidazo[2,1-b][1,3]thiazole-5-sulfonamide → HCID 178485216, Verbindung
https://huagongshe.com/reaction/1484451
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 6-Chloroimidazo[2,1-b][1,3]thiazole-5-sulfonamide | HCID 2779839 | — |
| Edukt | N-methyl-8-oxa-2,3-diaza-spiro[4.5]dec-3-ene-2-carboximidothioic acid methyl ester | HCID 67360788 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | HCID 178485216 | HCID 178485216 | 69% |
Reaktionsschritte
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).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09422244B2 |
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| Quelldatensatz | uspto-grants-2016_08 |
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| ORD ID | ord-efd19343a54c46ca985cd9c28e61078d |
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| Quellennotiz | uspto-grants-2016_08 |
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