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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | (S)-1-Boc-3-methylpiperazine | HCID 7023035 | — |
| 反応物 | 5-(((R)-oxiran-2-yl)methoxy)-2-methylbenzo[d]thiazole | HCID 21023606 | — |
| 溶媒 | 2-Methyl-2-butanol | HCID 6405 | — |
| 生成物 | tert-butyl 4-[(2R)-2-hydroxy-3-(2-methylbenzothiazol-5-yloxy)propyl](3S)-3-methylpiperazinecarboxylate | HCID 21023610 | 85.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07026321B2 |
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| 出典データセット | uspto-grants-2006_04 |
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| ORD ID | ord-bc1a07b020324c7683456ffc04116604 |
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| 出典メモ | uspto-grants-2006_04 |
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