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HRID 630323作成日:2026年10月27日

Acetic Acid → 1,1-Dimethylethyl 2-((4-(methoxycarbonyl)phenylmethylamino)methyl)-1-piperidinecarboxylate

https://huagongshe.com/reaction/630323

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Methyl 4-FormylbenzoateHCID 15294—
反応物tert-Butyl 2-(aminomethyl)piperidine-1-carboxylateHCID 2756482—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒WaterHCID 962—
溶媒1,1-DichloroethaneHCID 6365—
生成物1,1-Dimethylethyl 2-((4-(methoxycarbonyl)phenylmethylamino)methyl)-1-piperidinecarboxylateHCID 6848915796.6%

反応手順

A solution of 1-Boc-2-aminomethylpiperidine (429 mg, 2 mmol) and methyl 4-formylbenzoate (329 mg, 2 mmol) in dichloroethane (10 mL) was stirred as acetic acid (180 mg, 3 mmol) and sodium triacetoxyborohydride (487 mg, 2.3 mmol) were added sequentially. The reaction was stirred at ambient temperature for 17 hours. The reaction was poured into water and extracted with methylene chloride (2×). The organic phase was dried over sodium sulfate, filtered, and concentrated. Purification on silica gel using a gradient of ethyl acetate in hexane gave 0.7 g of 1,1-dimethylethyl 2-((4-(methoxycarbonyl)phenylmethylamino)methyl)-1-piperidinecarboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09315509B2
出典データセットuspto-grants-2016_04
ORD IDord-5fbca0966e384267abbd1bb71d88c92e
出典メモuspto-grants-2016_04