戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 407904作成日:2026年10月27日

(S)-tert-butyl 1-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)-2-oxopyrrolidin-3-ylcarbamate → (S)-3-amino-1-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)pyrrolidin-2-one

https://huagongshe.com/reaction/407904

反応式

関与物質

役割名称HCID仕込み量
反応物(S)-tert-butyl 1-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)-2-oxopyrrolidin-3-ylcarbamateHCID 86688087—
溶媒Trifluoroacetic acid methylene chlorideHCID 21863450—
生成物(S)-3-amino-1-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)pyrrolidin-2-oneHCID 67469717100%

反応手順

A solution of (S)-tert-butyl 1-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)-2-oxopyrrolidin-3-ylcarbamate (1 g, 2.6 mmol) in 50% TFA/CH2Cl2 (10 mL) was stirred at ambient temperature for 1 hour. The mixture was concentrated in vacuo. The residue was dissolved in CH2Cl2 (100 mL) and washed with 1N NaOH (100 mL) and brine. The combined organic layers were dried over MgSO4, filtered and concentrated in vacuo to yield (S)-3-amino-1-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)pyrrolidin-2-one (0.75 g, 2.6 mmol, 100%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754226B2
出典データセットuspto-grants-2014_06
ORD IDord-e65be34a4a12409591bf3f237b81c0a2
出典メモuspto-grants-2014_06