HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459442Generated: October 29, 2026
Methyl iodide → 5-Methyl-4,5,6,7-tetrahydrothiazolo(5,4-c)pyridine
https://huagongshe.com/reaction/459442
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Thiazolo[5,4-c]pyridine | HCID 14666228 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Methyl-4,5,6,7-tetrahydrothiazolo(5,4-c)pyridine | HCID 11186440 | — |
Reaction Steps
Thiazolo[5,4-c]pyridine (1.61 g) was dissolved in N,N-dimethylformamide (50 ml), and to the solution methyl iodide (1.50 ml) was added, the resultant mixture was stirred at 80° C. for 4 hours. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in methanol (100 ml), sodium borohydride (1.53 g) was added, and the resultant mixture was stirred at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure, and a saturated aqueous solution of potassium carbonate and ether were added to the residue to separate an organic layer. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by column chromatography on silica gel (dichloromethane:methanol=25:1) to obtain the title compound (1.28 g) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192968B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-a9e06777e3704e78af2ce984d829c01b |
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| Source note | uspto-grants-2007_03 |
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