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HRID 49446作成日:2026年10月24日

Ammonium Acetate → 1-(4-Aminopiperidin-1-yl)-3-phenylpropan-1-one

https://huagongshe.com/ja/reaction/49446

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium AcetateHCID 517165—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物1-(3-Phenylpropionyl)-4-ketopiperidineHCID 17817612—
溶媒MethanolHCID 887—
生成物1-(4-Aminopiperidin-1-yl)-3-phenylpropan-1-oneHCID 1679377247%

反応手順

To 3.2 g (13.8 mmol) of 135 in 125 mL of anhydrous methanol was added 21.3 g of ammonium acetate and 20 g of 3A molecular sieves. After stirring 30 min, 3.47 g (55.2 mmol) of sodium cyanoborohydride was added portionwise with stirring. After 3 hours, the mixture was gravity filtered, and the methanol evaporated under vacuum. The residue was partitioned between ice/HCl and ether. The acidic aqueous phase was extracted twice more with ether. The aqueous phase was made basic with ice and 50% aqueous NaOH. The mixture was extracted with CH2Cl2, dried, and evaporated under vacuum to give 1.5 g (47%) of the title amine 136. GC/MS indicated 100% purity with a molecular ion of 232.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06706740B2
出典データセットuspto-grants-2004_03
ORD IDord-08ae6f502bb042ebb1e5e2dd2d00758b
出典メモuspto-grants-2004_03