[H-].[Li+].[Al+3].[H-].[H-].[H-].[N:7]1([CH2:13][CH2:14][NH:15][C:16](=O)OC(C)(C)C)[CH2:12][CH:11]=[CH:10][CH2:9][CH2:8]1.[OH-].[Na+]>O1CCCC1>[N:7]1([CH2:13][CH2:14][NH:15][CH3:16])[CH2:8][CH:9]=[CH:10][CH2:11][CH2:12]180% Aluminum lithium hydride (0.36 g, 7.5 mmol) was suspended in tetrahydrofuran (10 mL). A solution of 1,1-dimethylethyl N-[2-(3,6-dihydropyridin-1(2H)-yl)ethyl]carbamate (0.68 g, 3.0 mmol) in tetrahydrofuran (10 mL) was added dropwise thereto at room temperature over 10 minutes, and the mixture was refluxed for 3 hours. The reaction solution was cooled to room temperature, and then a 1 N aqueous sodium hydroxide solution (20 mL) was added portionwise thereto. Insolubles were filtered off through a Celite, and the Celite was washed with tetrahydrofuran. The filtrate was concentrated under reduced pressure, and the residue was purified with amino silica gel column chromatography (hexane:ethyl acetate=19:1 to ethyl acetate) to obtain the title compound (0.18 g, yield 42%).
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