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HRID 221344作成日:2026年10月26日

Ammonia → 4-Carbamoylmethoxypiperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/221344

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物TriethylamineHCID 8471—
反応物Isobutyl chloroformateHCID 62365—
反応物2-((1-((Tert-butoxy)carbonyl)piperidin-4-yl)oxy)acetic acidHCID 1502082—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物4-Carbamoylmethoxypiperidine-1-carboxylic acid tert-butyl esterHCID 57856729—

反応条件

温度0 °C

反応手順

A solution of 4-carboxymethoxypiperidine-1-carboxylic acid tert-butyl ester (Preparation 1, 14.13 g, 54.7 mmol) and triethylamine (7.68 ml, 65.6 mmol) in anhydrous THF (250 ml) was cooled to 0° C. and isobutylchloroformate (8.51 ml, 65.6 mmol) introduced dropwise. After stirring at 0° C. for 30 min, the reaction mixture was cooled to −20° C. and added rapidly via cannula to a solution of 0.7M ammonia in anhydrous CH2Cl2 (250 ml, 180 mmol) at −70° C. The reaction was allowed to warm to rt and stirred for 1 h. The mixture was diluted with CH2Cl2 (250 ml) and washed with saturated aqueous NaHCO3 (200 ml), 0.5M HCl (200 ml) and brine (200 ml) then dried (MgSO4). The solvent was evaporated and the residue purified by flash chromatography IH-THF 3:7) to afford the title compound: δH (CDCl3) 1.49 (9H, s), 1.53-1.60 (2H, m), 1.85-1.92 (2H, m), 3.11 (2H, m), 3.58 (1H, m), 3.76-3.83 (2H, m), 3.98 (2H, s), 6.19 (1H, bs), 6.56 (1H, bs).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207147B2
出典データセットuspto-grants-2012_06
ORD IDord-90709735d32e4296963aec901ff714a8
出典メモuspto-grants-2012_06