HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076920Generated: November 1, 2026
Dimethyl Sulfoxide → 4-(Furan-2-yl)-N-(2-oxocyclohexyl)-1,3-thiazole-2-carboxamide
https://huagongshe.com/reaction/2076920
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4-(Furan-2-yl)-N-(2-hydroxycyclohexyl)-1,3-thiazole-2-carboxamide | HCID 67118892 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(Furan-2-yl)-N-(2-oxocyclohexyl)-1,3-thiazole-2-carboxamide | HCID 67118539 | 83% |
Reaction Steps
Oxalyl chloride (0.776 mL, 1.55 mol) and dimethyl sulfoxide (0.240 mL, 3.38 mmol) were dissolved in dichloromethane (3 mL), and the mixture was stirred at −60° C. for 10 minutes. To the solution was added 4-(2-furyl)-N-(2-hydroxycyclohexyl)thiazole-2-carboxamide (413 mg, 1.41 mmol) obtained in Step 1 and the mixture was stirred for 15 minutes. Triethylamine (0.983 mL, 7.05 mmol) was added to the mixture, and the mixture was stirred at room temperature for 10 minutes, then water and ethyl acetate were added thereto and the mixture was extracted. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was then evaporated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to give 4-(2-furyl)-N-(2-oxocyclohexyl)thiazole-2-carboxamide (339 mg, 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07928098B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-49a867885bce44ba88bd17531c4b521f |
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| Source note | uspto-grants-2011_04 |
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