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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546388Generated: November 1, 2026

Methyl iodide → 5-Methyl-4,5,6,7-tetrahydrothiazolo(5,4-c)pyridine

https://huagongshe.com/reaction/546388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantThiazolo[5,4-c]pyridineHCID 14666228—
SolventDimethylformamideHCID 6228—
Product5-Methyl-4,5,6,7-tetrahydrothiazolo(5,4-c)pyridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935824B2
Source datasetuspto-grants-2011_05
ORD IDord-bdedc9fc084f42eab05fab5db8c699ea
Source noteuspto-grants-2011_05