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Ethyl Acetate → 1-cyclopentyl N-[1-(tert-butoxycarbonyl)pyrrolidin-3-yl]-L-leucinate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Tert-butyl 3-oxopyrrolidine-1-carboxylate | HCID 471360 | — |
| 反応物 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 反応物 | L-leucine cyclopentyl ester tosylate | HCID 86633653 | — |
| 溶媒 | 1,1-Dichloroethane | HCID 6365 | — |
| 生成物 | 1-cyclopentyl N-[1-(tert-butoxycarbonyl)pyrrolidin-3-yl]-L-leucinate | HCID 86686416 | — |
反応手順
To a solution of N-tert-butoxycarbonyl-3-pyrrolidinone (0.382 g, 4.76 mmol) in dichloroethane (20 mL) was added L-leucine cyclopentyl ester tosylate (1.96 g, 5.3 mmol) and sodium triacetoxyborohydride (2.65 g, 12.5 mmol). The mixture was stirred at room temperature for 3 hours, then poured into ethyl acetate (150 mL) and quenched with saturated ammonium chloride solution (50 mL) and washed with saturated sodium hydrogen carbonate solution (3 times 30 mL). The organic extracts were dried (MgSO4), concentrated and purified by flash column chromatography (7:3 ethyl acetate:heptane) to yield the desired product. LC/MS: m/z 369.25 [M+H]+
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09321718B2 |
| 出典データセット | uspto-grants-2016_04 |
| ORD ID | ord-6da453aad4f84aac847932ee8559d33c |
| 出典メモ | uspto-grants-2016_04 |