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HRID 1795019作成日:2026年10月25日

(S)-1-Boc-3-methylpiperazine → tert-butyl 4-[(2R)-2-hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl](3S)-3-methylpiperazinecarboxylate

https://huagongshe.com/reaction/1795019

反応式

関与物質

役割名称HCID仕込み量
反応物(S)-1-Boc-3-methylpiperazineHCID 7023035—
反応物5-(((R)-oxiran-2-yl)methoxy)-2-methylbenzo[d]thiazoleHCID 21023606—
溶媒2-Methyl-2-butanolHCID 6405—
生成物tert-butyl 4-[(2R)-2-hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl](3S)-3-methylpiperazinecarboxylateHCID 2102361085.7%

反応条件

温度100 °C

反応手順

To a solution of 5-(((R)-oxiran-2-yl)methoxy)-2-methylbenzo[d]thiazole (3.24 g, 14.6 mmol) in tert-amyl alcohol (50 ml) was added (S)-tert-butyl 3-methylpiperazine-1-carboxylate (2.67 g, 13.3 mmol). The resulting mixture was stirred at 100° C. for 16 hours. It was then cooled, concentrated, and purified by chromatography (1:20 MeOH:CH2Cl2) to yield tert-butyl 4-[(2R)-2-hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl](3S)-3-methylpiperazinecarboxylate (4.8 g, 11.4 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07026321B2
出典データセットuspto-grants-2006_04
ORD IDord-bc1a07b020324c7683456ffc04116604
出典メモuspto-grants-2006_04