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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485041Generated: October 26, 2026

Propargyl bromide → 2-(N-methyl-N-propynylamino)benzothiazole

https://huagongshe.com/reaction/485041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantHexaneHCID 8058—
ReactantN-Methylbenzothiazol-2-amineHCID 28160—
ReactantButyllithiumHCID 178418339—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
Product2-(N-methyl-N-propynylamino)benzothiazoleHCID 2027133384%

Reaction Conditions

Temperature-78 °C

Reaction Steps

2-Methylaminobenzothiazole (c) (14.0 g) was dissolved in anhydrous tetrahydrofuran (250 ml) and a hexane solution (73 ml) of butyl lithium (6.53 g) was added thereto at -78° C. with stirring. The mixture was stirred for 1.5 hours under cooling and 2-propynyl bromide (8.4 ml) was dropwise added thereto. The resultant mixture was allowed to stand at room temperature overnight and then evaporated to remove the solvent. After addition of water, the residue was extracted with ether. The extract was washed with water, dried and evaporated to remove the solvent. The resultant residue was applied to column chromatography on silica gel (280 g) to give 2-(N-methyl-N-propynylamino)benzothiazole (d) (14.5 g, yield 84%) from chloroform eluate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04535088
Source datasetuspto-grants-1985_08
ORD IDord-655eb8d90eae40d1a7ee035d7ffa7030
Source noteuspto-grants-1985_08