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HRID 733092作成日:2026年10月25日

Acetic Acid → Methyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}piperidin-1-yl)methyl]cyclobutanecarboxylate

https://huagongshe.com/reaction/733092

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Sodium BicarbonateHCID 516892—
反応物Tert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物Methyl 1-formylcyclobutane-1-carboxylateHCID 15656335—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}piperidin-1-yl)methyl]cyclobutanecarboxylateHCID 6723339183.2%

反応条件

温度60 °C

反応手順

To a stirred mixture of tert-butyl(piperidin-4-ylmethyl)carbamate (12.8 g, 60 mmol) and methyl 1-formylcyclobutanecarboxylate (2.13 g, 15 mmol, Davis, Charles R.; Swenson, Dale C.; Burton, Donald J., J. Org. Chem., 1993, 58, 6843) in tetrahydrofuran (50 mL) was added acetic acid (8.6 mL, 150 mmol) at ambient temperature. After 30 min, sodium triacetoxyborohydride (12.7 g, 60 mmol) was added to the mixture. Then, the mixture was heated to 60° C. for 2 h. After cooling, the reaction mixture was poured into sat. NaHCO3 aq. The aqueous layer was extracted with CH2Cl2 for 3 times. The combined organic phase were washed with brine, dried over MgSO4, filtered and concentrated. The residue was chromatographed on a column of silica gel eluting with hexane/ethyl acetate (1:1) to give 4.25 g (83%) of the title compound as white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07589109B2
出典データセットuspto-grants-2009_09
ORD IDord-7d351ffb7d2645e6b188a7254df7a931
出典メモuspto-grants-2009_09