Water → (S)-1-(7-chloro-5-(4-chlorophenyl)-2-methylquinolin-6-yl)ethane-1,2-diol
반응식
CC[C@H]1[C@H]2C[C@H]([C@H](OC3C4C(=CC=CC=4)C(O[C@H](C4C=CN=C5C=4C=C(OC)C=C5)[C@@H]4N5C[C@H](CC)[C@@H](CC5)C4)=NN=3)C3C=CN=C4C=3C=C([O:22]C)C=C4)N(CC2)C1.[C:59]([OH:63])(C)([CH3:61])[CH3:60].O.[Cl:65][C:66]1[CH:75]=[C:74]2[C:69]([CH:70]=[CH:71][C:72]([CH3:76])=[N:73]2)=[C:68]([C:77]2[CH:82]=[CH:81][C:80]([Cl:83])=[CH:79][CH:78]=2)C=1C=C>C(OCC)(=O)C>[Cl:65][C:66]1[CH:75]=[C:74]2[C:69]([CH:70]=[CH:71][C:72]([CH3:76])=[N:73]2)=[C:68]([C:77]2[CH:82]=[CH:81][C:80]([Cl:83])=[CH:79][CH:78]=2)[C:60]=1[C@H:59]([OH:63])[CH2:61][OH:22]참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
AD-mix-α (1 g, excess) was added to a mixed solvent of t-butanol and water (4 mL/4 mL) and stirred at room temperature for 5 min and cooled to 0° C. The mixture was transferred to another flask containing 7-chloro-5-(4-chlorophenyl)-2-methyl-6-vinylquinoline (1G) (30 mg, 0.096 mmol) and stirred at 0° C. for 16 hours. The mixture was diluted with ethyl acetate, washed with NaHCO3 solution, water and brine, dried over Na2SO4, filtered and concentrated in vacuo. The obtained residue was purified by flash chromatography to provide the desired product 1H (28 mg, 84%). LCMS-ESI+ (m/z): 348.2, 350.2 (M+H)+.
후처리
- temperaturecooled to 0° C
- customThe mixture was transferred to another flask
- stirringstirred at 0° C. for 16 hours
- washwashed with NaHCO3 solution, water and brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe obtained residue was purified by flash chromatography
출처 및 근거
- ORD 기록
- ord-5c815a5d76614fe789dcfaa6924e0a9a
- 출처 데이터셋
- uspto-grants-2016_03
- 특허 번호
- US09296758B2
반응 노트
불러오는 중…