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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| 反応物 | 2-Methyl-5-(oxiran-2-ylmethoxy)benzothiazole | HCID 9920872 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | tert-butyl 4-[(2R)-2-hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl]piperazinecarboxylate | HCID 29943209 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07452889B2 |
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| 出典データセット | uspto-grants-2008_11 |
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| ORD ID | ord-f89ae0bb8828413c872affa46c79765a |
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| 出典メモ | uspto-grants-2008_11 |
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