HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568293Generated: October 29, 2026
Thionyl Chloride → HCID 21262359, compound
https://huagongshe.com/reaction/568293
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 21262429 | HCID 21262429 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21262359 | HCID 21262359 | — |
Reaction Steps
3-Hydroxymethyl-5-methylimidazo[5,1-b]thiazolehydrochloride (1.10 g) is suspended in 20 ml of THF, 0.7 ml of thionyl chloride is added thereto, and the mixture is stirred at 85° C. for 3.5 hr. The solvent is removed by evaporation to give 1.10 g of 3-chloromethyl-5-methylimidazo[5,1-b]thiazolehydrochloride. This compound is dissolved in 7 ml of DMF, 1.36 g of triphenylphosphine is added thereto, and the mixture is stirred at 83° C. for 15 hr and at 90° C. for 4 hr. The resultant precipitate is collected by filtration and washed with diethyl ether to give 1.87 g of (5-methylimidazo[5,1-b]thiazol-3-yl)methyltriphenylphosphonium chloride hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06180622B2 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-dddfb79fd9314c718f0bf68916d15f45 |
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| Source note | uspto-grants-2001_01 |
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