HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484451Generated: October 25, 2026
6-Chloroimidazo[2,1-b][1,3]thiazole-5-sulfonamide → HCID 178485216, compound
https://huagongshe.com/reaction/1484451
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Chloroimidazo[2,1-b][1,3]thiazole-5-sulfonamide | HCID 2779839 | — |
| Reactant | N-methyl-8-oxa-2,3-diaza-spiro[4.5]dec-3-ene-2-carboximidothioic acid methyl ester | HCID 67360788 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178485216 | HCID 178485216 | 69% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422244B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-efd19343a54c46ca985cd9c28e61078d |
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| Source note | uspto-grants-2016_08 |
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