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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352875Generated: October 30, 2026

Methyl iodide → 5-Methyl-4,5,6,7-tetrahydrothiazolo[4,5-c]pyridine

https://huagongshe.com/reaction/352875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantThiazolo[4,5-c]pyridineHCID 585837—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-Methyl-4,5,6,7-tetrahydrothiazolo[4,5-c]pyridineHCID 11378622—

Reaction Conditions

Temperature80 °C

Reaction Steps

In N,N-dimethylformamide (80 ml) was dissolved thiazolo[4,5-c]pyridine (700 mg), followed by the addition of methyl iodide (0.65 ml). The resulting mixture was stirred under heat at 80° C. for 4 hours. After concentration of the reaction mixture under reduced pressure, the residue was dissolved in water (100 ml). Sodium borohydride (583 mg) was added to the resulting solution, followed by stirring at room temperature for 1 hour. After the addition of a saturated aqueous solution of potassium carbonate, the resulting mixture was extracted with ether. The organic layer thus extracted was dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column (methylene chloride:methanol=25:1), whereby the title compound (596 mg) was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747023B1
Source datasetuspto-grants-2004_06
ORD IDord-ede08ee8c3084a36a44ca0dd9c3f63a0
Source noteuspto-grants-2004_06