HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989816Generated: October 30, 2026
Hydrochloride methanol → HCID 23449075, compound
https://huagongshe.com/reaction/989816
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Reactant | HCID 23449280 | HCID 23449280 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23449075 | HCID 23449075 | — |
Reaction Steps
A 10% hydrochloric acid/methanol solution (1 ml) and 120 mg of 10%Pd-C were added to a solution of 0.44 g of 7-azidoacetylimidazo[5,1-b]thiazole in 50 ml of methanol and 50 ml of THF. The atmosphere in the reactor was replaced with hydrogen. The system was stirred at room temperature for 2 hr. The reaction mixture was filtered. The solvent was removed by distillation. To the residue were added 10 ml of DMF, 0.39 g of 4-nitrophenyl formate, and 0.66 ml of triethylamine. The mixture was stirred at room temperature for 30 min. Dichloromethane was added to the reaction solution. The mixture was washed with water and saturated brine in that order, and then dried over anhydrous magnesium sulfate. The solvent was removed by distillation. The residue was purified by column chromatography on silica gel (dichloromethane:methanol=10:1) to give 0.24 g of 7-formylaminoacetylimidazo[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-1424634d09004d749179f487e013b979 |
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| Source note | uspto-grants-2002_10 |
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