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HRID 271223作成日:2026年10月27日

tert-Butyl piperazine-1-carboxylate → tert-butyl 4-[(2R)-2-hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]piperazinecarboxylate

https://huagongshe.com/reaction/271223

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2-Methyl-5-(oxiran-2-ylmethoxy)benzothiazoleHCID 9920872—
溶媒EthanolHCID 702—
生成物tert-butyl 4-[(2R)-2-hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]piperazinecarboxylateHCID 29943209—

反応条件

温度85 °C

反応手順

To 2-methyl-5-(oxiran-2-ylmethoxy) benzothiazole (2.21 g, 10 mmol), a compound of formula (3), was added tert-butyl 1-piperazinecarboxylate (1.86 g, 10 mmol), a compound of formula (4), and ethanol (30 ml). The resulting solution was heated to 85° C. and stirred for 8 hours. The solvent was evaporated under reduced pressure, and the residue was chromatographed on silica gel, eluting with 5% methanol/methylene chloride, to yield tert-butyl 4-[(2R)-2-hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]piperazinecarboxylate as a clear oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07452889B2
出典データセットuspto-grants-2008_11
ORD IDord-f89ae0bb8828413c872affa46c79765a
出典メモuspto-grants-2008_11