Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260634Generated: November 1, 2026

Methyl iodide → N-Methyl-1,3-benzothiazol-6-amine

https://huagongshe.com/reaction/2260634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 18998810HCID 18998810—
SolventAcetoneHCID 180—
ProductN-Methyl-1,3-benzothiazol-6-amineHCID 1063086019%

Reaction Steps

To 6-Trifluoroacetamidobenzothiazole (1.97 g, 8 mmol) in 40 ml dry acetone was added methyl iodide (4.54 g, 32 mmol) and then KOH (2.1 g, 32 mmol). The mixture was refluxed for 40 min. and concentrated in vacuo. The product was taken up in 40 ml H2O, refluxed for 40 min. and extracted with methylene chloride. The organic phase was washed with water, dried over Na2SO4 and concentrated in vacuo. The product was purified by flash chromatography (silica gel, methylene chloride) to give 250 mg 6-methylamino-benzothiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05478845
Source datasetuspto-grants-1995_12
ORD IDord-3cac699a41a841f3ba23cbb621c2d77f
Source noteuspto-grants-1995_12