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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloroimidazo[2,1-b][1,3]thiazole-5-sulfonamideHCID 2779839—
ReactantN-methyl-8-oxa-2,3-diaza-spiro[4.5]dec-3-ene-2-carboximidothioic acid methyl esterHCID 67360788—
SolventAcetonitrileHCID 6342—
ProductHCID 178485216HCID 17848521669%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422244B2
Source datasetuspto-grants-2016_08
ORD IDord-efd19343a54c46ca985cd9c28e61078d
Source noteuspto-grants-2016_08