HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839317Generated: October 26, 2026
Formamide → 7-(Thiazol-4-yl)imidazo[5,1-b]thiazole
https://huagongshe.com/reaction/1839317
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formamide | HCID 713 | — |
| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 7-Chloroacetylimidazo[5,1-b]thiazole | HCID 23449333 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-(Thiazol-4-yl)imidazo[5,1-b]thiazole | HCID 23449111 | — |
Reaction Steps
Diphosphorus pentasulfide (846 mg) was added to 8.4 ml of formamide. The mixture was stirred at room temperature overnight. 7-Chloroacetylimidazo[5,1-b]thiazole (2.32 g) was added to the reaction solution. The mixture was stirred at room temperature for 15 hr. Water (20 ml) and 10 ml of dichloromethane were added thereto The mixture was adjusted to pH 8.8 by gradually adding a sodium hydrogencarbonate powder. Extraction was carried out six times with 50 ml of dichloromethane. The organic layer 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 (hexane ethyl acetate=1 2) to give 1.72 g of 7-(thiazol-4-yl)imidazo[5,1-b]thiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06677331B2 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-bce039e24e1c45d9ae4c5bc3e30871fc |
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| Source note | uspto-grants-2004_01 |
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