戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 585064作成日:2026年10月26日

Trifluoroacetic acid methylene chloride → 1-(2-Methylbenzothiazol-5-yloxy)-3-piperazin-1-ylpropan-2-ol

https://huagongshe.com/reaction/585064

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acid methylene chlorideHCID 21863450—
反応物4-[2-Hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]-piperazine-1-carboxylic acid tert-butyl esterHCID 21935528—
溶媒AcetoneHCID 180—
溶媒Potassium CarbonateHCID 11430—
生成物1-(2-Methylbenzothiazol-5-yloxy)-3-piperazin-1-ylpropan-2-olHCID 21911691—

反応手順

A solution of 4-[2-hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]-piperazine-1-carboxylic acid tert-butyl ester, a compound of formula (5) (2.0 g, 4.9 mmol), and 25% trifluoroacetic acid/methylene chloride (20 ml) was allowed to stir at room temperature overnight. The solvent was evaporated (in vacuo) to yield an oil. The oil was diluted with acetone (20 ml) and solid potassium carbonate was added until the foaming stopped. The resulting mixture was allowed to stir overnight. The solution was filtered through Celite 512, and the filtrate was evaporated (in vacuo), to yield an oil. The oil was placed under high vacuum overnight, to yield 1-(2-methylbenzothiazol-5-yloxy)-3-piperazin-1-ylpropan-2-ol, as a clear viscous oil (3.4 g. 6.3 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06930111B2
出典データセットuspto-grants-2005_08
ORD IDord-d07b9fcd9cd9436785e486ee7507f440
出典メモuspto-grants-2005_08