HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603476Generated: November 1, 2026
Allyl chloroformate → HCID 19605026, compound
https://huagongshe.com/reaction/1603476
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl chloroformate | HCID 18052 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 15428311 | HCID 15428311 | — |
| Reactant | HCID 19605154 | HCID 19605154 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19605026 | HCID 19605026 | — |
Reaction Steps
To 207 mg of a mixture of 3-(N-methylamino)methylimidazo[5,1-b]thiazole and 3-hydroxymethylimidazo[5,1-b]thiazole in a ratio of about 1:1, 10 ml of dichloromethane and 3 ml of water were added, and then 0.092 ml of allyl chloroformate was added thereto under ice-cooling. The mixture was stirred for 30 minutes under ice-cooling, while the aqueous layer was adjusted to pH 8.5 by adding a sodium hydrogencarbonate solution. The organic layer was separated, and the aqueous layer was extracted with dichloromethane. The combined organic layer was dried over anhydrous magnesium sulfate and then filtered, and the solvent was evaporated under reduced pressure. The resulting residue was purified by a silica gel column chromatograph to obtain 73.6 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05990101 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-cceee729e7dc43f9b5b1be37e531002f |
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| Source note | uspto-grants-1999_11 |
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