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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

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 numberUS07192968B2
Source datasetuspto-grants-2007_03
ORD IDord-a9e06777e3704e78af2ce984d829c01b
Source noteuspto-grants-2007_03