関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonium Hydroxide | HCID 14923 | — |
| 反応物 | Ethanol, 2-[2-[2-(2-aminoethoxy)ethoxy]ethoxy]- | HCID 160103 | — |
| 反応物 | 2,5-Dioxopyrrolidin-1-yl 3-(tritylthio)propanoate | HCID 17935426 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-(2-{2-[2-(2-hydroxyethoxy)ethoxy]ethoxy}ethyl)-3-(tritylthio)propanamide | HCID 68927996 | 82.7% |
反応手順
Succinimido 3-(triphenylmethylthio)propanoate (4.06 mg, 9.12 mmol) was added to a 0° C. solution of 2-{2-[2-(2-aminoethoxy)ethoxy]ethoxy}ethanol (C. Bertozzi and M. Bednarski, J. Org. Chem. 1991, 56, 4326-4329) (9.12 mmol) in dichloromethane (20 mL). The solution was stirred at room temperature for 2 days and concentrated ammonium hydroxide (1 mL) was added. After 20 minutes, the mixture was filtered and the filtrate was subjected to an extractive workup. The organic layer were dried over sodium sulfate and concentrated under reduced pressure. The crude product was purified by HPFC on silica gel (gradient elution with 2-19% CMA in chloroform) to provide 3.95 g of N-(2-{2-[2-(2-hydroxyethoxy)ethoxy]ethoxy}ethyl)-3-(tritylthio)propanamide as a colorless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08951528B2 |
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| 出典データセット | uspto-grants-2015_02 |
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| ORD ID | ord-2dd8f0e9717841589cc67d31e5e128d2 |
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| 出典メモ | uspto-grants-2015_02 |
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