Diisobutylaluminumhydride → 1-(5-nitro-3-pyridin-2-yl-3,4-dihydro-2H-1,4-benzoxazin-3-yl)methanamine
反応式
[H-].C([Al+]CC(C)C)C(C)C.[N+:11]([C:14]1[C:19]2[NH:20][C:21]([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][N:27]=3)([C:24]#[N:25])[CH2:22][O:23][C:18]=2[CH:17]=[CH:16][CH:15]=1)([O-:13])=[O:12]>C1(C)C=CC=CC=1>[N+:11]([C:14]1[C:19]2[NH:20][C:21]([CH2:24][NH2:25])([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][N:27]=3)[CH2:22][O:23][C:18]=2[CH:17]=[CH:16][CH:15]=1)([O-:13])=[O:12]参加物
4
実験手順
1.0 M Diisobutylaluminum hydride in toluene (200 μL, 0.2 mmol) was added drop-wise to a solution of 5-nitro-3-pyridin-2-yl-3,4-dihydro-2H-1,4-benzoxazine-3-carbonitrile (50 mg, 0.2 mmol) (Example 71, Step 1), in toluene (5 mL) at room temperature. The reaction mixture was stirred for 10 min, then quenched with methanol. The resulting mixture was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate. The organic layer was washed with brine, dried over magnesium sulfate, filtered, and concentrated to give crude 1-(5-nitro-3-pyridin-2-yl-3,4-dihydro-2H-1,4-benzoxazin-3-yl)methanamine solid (0.05 g. 100%). LCMS calculated for C14H15N4O3 (M+H)+: m/z=287.1. found: 287.1.