HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989809Generated: October 26, 2026
Dimethylformamide → Imidazo(4,3-b)(1,3)thiazole-7-carbaldehyde
https://huagongshe.com/reaction/989809
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Imidazo[5,1-b]thiazole | HCID 21262404 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Imidazo(4,3-b)(1,3)thiazole-7-carbaldehyde | HCID 22390357 | — |
Reaction Steps
DMF (15.48 ml) was added to 80 ml of dichloromethane. A solution of 18.32 ml of phosphorus oxychloride in 80 ml of dichloromethane was dropwise added thereto under ice cooling. A reaction was allowed to proceed at room temperature for 30 min. A solution of imidazo[5,1-b]thiazole in 40 ml of dichloromethane was added dropwise thereto. The mixture was heated under reflux for 2.5 hr. The reaction solution was poured into ice. The reaction solution was adjusted to pH 9.8 by the addition of a 5 N aqueous sodium hydroxide solution, followed by extraction five times with 200 ml of dichloromethane. The extract was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by column chromatography on silica gel (eluting with dichloromethane:ethyl acetate=5:1, ethyl acetate alone, and then dichloromethane:methanol=10:1) to give 2.37 g of 7-formylimidazo[5,1-b]thiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06458780B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-bab04d02ccfc4ebabe9ce8d200887d31 |
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| Source note | uspto-grants-2002_10 |
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