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HRID 1632009作成日:2026年10月25日
Diisopropylethylamine → (S)-22-(tert-Butoxycarbonyl)-45,45-dimethyl-10,19,24,43-tetraoxo-3,6,12,15,44-pentaoxa-9,18,23-triazahexatetracontanoic acid
https://huagongshe.com/reaction/1632009
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 17-Amino-10-oxo-3,6,12,15-tetraoxa-9-azaheptadecanoic acid | HCID 51340918 | — |
| 反応物 | 2-(19-tert-Butoxycarbonylnonadecanoylamino)pentanedioic acid 1-tert-butyl ester 5-(2,5-dioxopyrrolidin-1-yl)ester | HCID 86644530 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | (S)-22-(tert-Butoxycarbonyl)-45,45-dimethyl-10,19,24,43-tetraoxo-3,6,12,15,44-pentaoxa-9,18,23-triazahexatetracontanoic acid | HCID 86644529 | 96% |
反応手順
To a solution of 2-(19-tert-Butoxycarbonylnonadecanoylamino)pentanedioic acid 1-tert-butyl ester 5-(2,5-dioxopyrrolidin-1-yl) ester (2.50 g) and [2-(2-{2-[2-(2-aminoethoxy)ethoxy]acetylamino}ethoxy)ethoxy]acetic acid (alternative name: H-OEG-OEG-OH)(1.47 g) in ethanol (40 ml) was added DIPEA (1.26 ml). The mixture was stirred at room temperature overnight and then concentrated in vacuo. To the residue was added aqueous 0.1 N HCl (150 ml) and ethyl acetate (200 ml). The layers were separated and the aqueous layer was extracted with ethyl acetate (100 ml). The combined organic layers were washed with water and brine, dried (magnesium sulphate) and concentrated in vacuo to give an oil, which crystallised on standing. Yield 96% (3.1 g). LCMS: Theoretical mass: 874.2. Found: 874.49.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08791236B2 |
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| 出典データセット | uspto-grants-2014_07 |
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| ORD ID | ord-40579ac7e02c41dabeba5d3bee73265a |
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| 出典メモ | uspto-grants-2014_07 |
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