戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 60900作成日:2026年10月26日

Carbamate → (2S,3R)-Allyl 2-(aminomethyl)-3-methylpiperidine-1-carboxylate

https://huagongshe.com/reaction/60900

反応式

関与物質

役割名称HCID仕込み量
反応物CarbamateHCID 276—
反応物Allyl chloroformateHCID 18052—
反応物Hydrazine hydrate (1:1)HCID 24654—
反応物DiisopropylethylamineHCID 81531—
反応物2-(((2S,3R)-3-Methylpiperidin-2-yl)methyl)isoindoline-1,3-dioneHCID 117727630—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物(2S,3R)-Allyl 2-(aminomethyl)-3-methylpiperidine-1-carboxylateHCID 89748216—

反応手順

To a solution of 2-(((2S,3R)-3-methylpiperidin-2-yl)methyl)isoindoline-1,3-dione (5 g, 19.4 mmol) in CH2Cl2 at 0° C. was added DIPEA (3.8 mL), followed by allyl chloroformate (2.6 mL). The reaction was allowed to warm to rt overnight. After 16 h, the reaction was concentrated to remove the CH2Cl2, and then re-suspended in EtOAc and washed with 1 M HCl (2×), brine (2×), dried (MgSO4) and concentrated to give the crude carbamate which was used without further purification. A mixture of the crude carbamate and hydrazine hydrate (2 g, 39 mmol) in MeOH (100 mL) was heated at 60° C. for 2 h. The mixture was cooled to rt and the solvent was removed in vacuo. The crude was dissolved in EtOAc and washed with 2 N NaOH (2×), brine, and then dried (Na2SO4). The solvent was removed in vacuo to obtain the title compound which was used without further purification. ESI-MS (m/z): 213 [M+1]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440982B2
出典データセットuspto-grants-2016_09
ORD IDord-fbf016bb74e441ada4a45e7d402b144f
出典メモuspto-grants-2016_09