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HRID 891059作成日:2026年10月26日

Dichloromethane → (2S)-1-(2-methylbenzothiazol-5-yloxy)-3-(4-prop-2-ynylpiperazinyl)propan-2-ol

https://huagongshe.com/reaction/891059

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Propargyl bromideHCID 7842—
反応物Potassium CarbonateHCID 11430—
反応物(2S)-1-(2-methylbenzothiazol-5-yloxy)-3-piperazinylpropan-2-olHCID 58595334—
溶媒AcetoneHCID 180—
溶媒MethanolHCID 887—
生成物(2S)-1-(2-methylbenzothiazol-5-yloxy)-3-(4-prop-2-ynylpiperazinyl)propan-2-olHCID 5859532955.7%

反応手順

To a solution of (2S)-1-(2-methylbenzothiazol-5-yloxy)-3-piperazinylpropan-2-ol (800 mg, 2.6 mmol) in acetone (20 ml) was added propargyl bromide (80% solution, 0.290 ml, 2.6 mmol) and potassium carbonate (720 mg, 5.2 mmol). The solution was heated to reflux and stirred for 5 hours. Thin layer chromatography (10:1 dichloromethane:methanol) showed formation of product. The solution was cooled and filtered. The filtrate was concentrated and purified by preparative chromatography (dichloromethane:methanol) to yield (2S)-1-(2-methylbenzothiazol-5-yloxy)-3-(4-prop-2-ynylpiperazinyl)propan-2-ol (500 mg, M+1=346.2). B. Preparation of a Compound of Formula I

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07001909B2
出典データセットuspto-grants-2006_02
ORD IDord-15213026c77949888525af9651d98d57
出典メモuspto-grants-2006_02