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HRID 603248作成日:2026年10月27日
Sodium Bicarbonate → N-(3,4-Dichlorophenyl)-4-{[(2R)-4-tert-butoxycarbonylpiperazin-2-yl]carbonyl}piperazine-1-carboxamide
https://huagongshe.com/reaction/603248
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | PyBOP | HCID 2724699 | — |
| 反応物 | N-(3,4-Dichlorophenyl)piperazine-1-carboxamide | HCID 16775732 | — |
| 反応物 | (2R)-1-(tert-Butoxycarbonyl)piperazine-2-carboxylic acid | HCID 24820285 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | N-(3,4-Dichlorophenyl)-4-{[(2R)-4-tert-butoxycarbonylpiperazin-2-yl]carbonyl}piperazine-1-carboxamide | HCID 67220684 | — |
反応手順
N-(3,4-Dichlorophenyl)piperazine-1-carboxamide (596 mg) and (2R)-1-BOC-piperazine-2-carboxylic acid (500 mg) were dissolved in N,N-dimethylformamide (30 ml) and stirred at 0° C. Triethylamine (0.61 ml) was added followed by PYBOP reagent (1.13 g). The mixture was allowed to warm to room temperature overnight, poured into saturated aqueous sodium bicarbonate (60 ml) and extracted with ethyl acetate (2×100 ml), adding a little water during the process to dissolve precipitated sodium bicarbonate. The combined organic extracts were treated with brine (100 ml), dried (sodium sulphate), concentrated in vacuo and adsorbed onto silica for purification by chromatography eluting with 0-15% methanol dichloromethane. This gave the product as a white glass (710 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07906645B2 |
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| 出典データセット | uspto-grants-2011_03 |
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| ORD ID | ord-71bb2a4bc7e54ee7b5d2025d10f96c61 |
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| 出典メモ | uspto-grants-2011_03 |
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