HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376608Generated: October 26, 2026
Formic Acid → 3-(Formylamino)methylimidazo[5,1-b]thiazole
https://huagongshe.com/reaction/1376608
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Aminomethylimidazo[5,1-b]thiazole | HCID 19605155 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(Formylamino)methylimidazo[5,1-b]thiazole | HCID 19605025 | 87% |
Reaction Steps
0.33 g of the above-obtained 3-aminomethylimidazo[5,1-b]-thiazole was dissolved in 10 ml of dichloromethane. To this solution, a mixture which had been prepared in advance by reacting 0.5 ml of formic acid with 0.5 ml of acetic anhydride at 50° C. for 10 minutes was added with stirring, and the resulting mixture was stirred at room temperature for an additional one hour. To the reaction solution was added 20 ml of a saturated aqueous solution of sodium hydrogencarbonate, and the organic layer was separated. The aqueous layer was extracted with dichloromethane (10 ml×2). The combined organic layers were dried over anhydrous magnesium sulfate, and concentrated to dryness under reduced pressure to give 0.338 g (yield 87%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05663162 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-f00eba499cae41e48c43b10f161cb31e |
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| Source note | uspto-grants-1997_09 |
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