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HRID 485041作成日:2026年10月25日

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

https://huagongshe.com/reaction/485041

反応式

関与物質

役割名称HCID仕込み量
反応物Propargyl bromideHCID 7842—
反応物HexaneHCID 8058—
反応物N-Methylbenzothiazol-2-amineHCID 28160—
反応物ButyllithiumHCID 178418339—
溶媒ChloroformHCID 6212—
溶媒TetrahydrofuranHCID 8028—
生成物2-(N-methyl-N-propynylamino)benzothiazoleHCID 2027133384%

反応条件

温度-78 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04535088
出典データセットuspto-grants-1985_08
ORD IDord-655eb8d90eae40d1a7ee035d7ffa7030
出典メモuspto-grants-1985_08