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HRID 1046302作成日:2026年10月26日

Acetic Acid → 1,1-Dimethylethyl 2-[[[[4-(methoxycarbonyl)phenyl]methyl]amino]methyl]-1-pyrrolidinecarboxylate

https://huagongshe.com/reaction/1046302

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Sodium BicarbonateHCID 516892—
反応物(+-)-2-(Aminomethyl)-1-N-Boc-pyrrolidineHCID 2756484—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒1,1-DichloroethaneHCID 6365—
生成物1,1-Dimethylethyl 2-[[[[4-(methoxycarbonyl)phenyl]methyl]amino]methyl]-1-pyrrolidinecarboxylateHCID 6849038945.9%

反応手順

A solution of 1,1-dimethylethyl 2-(aminomethyl)-1-pyrrolidinecarboxylate (1000 mg, 5 mmol) and methyl 4-formylbenzoate (820 mg, 5 mmol) in dichloroethane was stirred as acetic acid (450 mg, 7.5 mmol) and sodium triacetoxyborohydride (1271 mg, 6 mmol) were added sequentially at ambient temperature. After stirring at ambient temperature for 17 hours, treated with a saturated aqueous solution of sodium bicarbonate and extracted with EtOAc. The combined organic extracts were dried and concentrated. Purification by flash chromatography afforded 1,1-dimethylethyl 2-[[[[4-(methoxycarbonyl)phenyl]methyl]amino]methyl]-1-pyrrolidinecarboxylate (800 mg), 1H NMR (CDCl3) 7.98 (d, 2H), 3.37 (d, 2H), 3.91 (s, 3H), 3.82 (s, 2H), 3.36 (m, 2H), 2.72 (m, 1H), 1.82 (m, 3H), 1.44 (m, 2H) ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08569303B2
出典データセットuspto-grants-2013_10
ORD IDord-c7cf57319bf84ee9b19b713de02417ab
出典メモuspto-grants-2013_10