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HRID 891050作成日:2026年10月26日

tert-Butyl piperazine-1-carboxylate → (2S)-1-(2-methylbenzothiazol-5-yloxy)-3-piperazinylpropan-2-ol

https://huagongshe.com/reaction/891050

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
反応物Trifluoroacetic acid methylene chlorideHCID 21863450—
反応物(2S)-1-(2-methylbenzothiazol-5-yloxy)butan-2-olHCID 69622255—
溶媒AcetoneHCID 180—
溶媒Potassium CarbonateHCID 11430—
生成物(2S)-1-(2-methylbenzothiazol-5-yloxy)-3-piperazinylpropan-2-olHCID 58595334—

反応手順

A solution of (2S)-1-(2-methylbenzothiazol-5-yloxy)butan-2-ol, tert butyl piperazinecarboxylate, 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 (2S)-1-(2-methylbenzothiazol-5-yloxy)-3-piperazinylpropan-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US07001909B2
出典データセットuspto-grants-2006_02
ORD IDord-ae629f88f1d64d689a9a55ca7f320969
出典メモuspto-grants-2006_02