HCID 66980987、化合物 → HCID 67130097、化合物

反応式

[CH3:1][C:2]1[C:3]([C:37]([F:40])([F:39])[F:38])=[C:4]([CH:7]=[CH:8][C:9]=1[N:10]1[C@@H:14]([CH2:15][O:16]C(C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[CH2:13][CH2:12][C:11]1=[O:36])[C:5]#[N:6]>O1CCOCC1.Cl.O>[OH:16][CH2:15][C@H:14]1[CH2:13][CH2:12][C:11](=[O:36])[N:10]1[C:9]1[CH:8]=[CH:7][C:4]([C:5]#[N:6])=[C:3]([C:37]([F:40])([F:38])[F:39])[C:2]=1[CH3:1]

参加物

実験手順

To a solution of (R)-3-methyl-4-(2-oxo-5-((trityloxy)methyl)pyrrolidin-1-yl)-2-(trifluoromethyl)benzonitrile (3h) (0.48 g, 0.93 mmol) in 1,4-dioxane (15 mL), 2M HCl in 1,4-dioxane (5 mL) was added at 0° C. and stirred for 4 h. After completion of reaction (by TLC), the reaction mixture was diluted with water (20 mL) and extracted with EtOAc (2×15 mL). The combined organic extracts were washed with water (2×30 mL), dried over Na2SO4 and concentrated under reduced pressure to obtain the crude compound was purified by column chromatography to provide the alcohol 3i (0.22 g, 79%) as a white solid.