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HRID 16596作成日:2026年10月24日

tert-Butyl acrylate → tert-butyl 3-[4-({[(3-isopropyl-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)carbonyl]amino}methyl)piperidin-1-yl]propanoate

https://huagongshe.com/ja/reaction/16596

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl acrylateHCID 15458—
反応物3-isopropyl-2-oxo-N-(piperidin-4-ylmethyl)-2,3-dihydro-1H-benzimidazole-1-carboxamideHCID 44249188—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium BicarbonateHCID 516892—
生成物tert-butyl 3-[4-({[(3-isopropyl-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)carbonyl]amino}methyl)piperidin-1-yl]propanoateHCID 6858576016%

反応手順

A mixture of 3-isopropyl-2-oxo-N-(piperidin-4-ylmethyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide (0.50 g, 1.58 mmol, Step 2), tert-butyl acrylate (0.340 mL, 2.37 mmol) and iPrNEt (0.275 mL, 2.37 mmol) in THF (20 mL) was refluxed for 18 h. After cooling, the reaction mixture was diluted with sat. NaHCO3 aq. (100 mL), extracted with CH2Cl2 (100 mL) for three times. The combined extracts were dried over Na2SO4, filtered and concentrated. The residue was chromatographed on a column of silica gel eluted with MeOH/CH2Cl2 (1:20→1:10) and then NH-silica gel eluted with EtOAc/hexane (1:5→1:2) to give 0.111 g (16%) of title compound as colorless syrup.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737163B2
出典データセットuspto-grants-2010_06
ORD IDord-0f9e13c6d3304deea6cdd84e880c7264
出典メモuspto-grants-2010_06