Water → (S)-1-(7-chloro-5-(4-chlorophenyl)-2-methylquinolin-6-yl)ethane-1,2-diol

HRID 931702ノート

反応式

HRID 931702 の反応式
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]

参加物

6

実験手順

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)+.

後処理

  1. temperaturecooled to 0° C
  2. customThe mixture was transferred to another flask
  3. stirringstirred at 0° C. for 16 hours
  4. washwashed with NaHCO3 solution, water and brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe obtained residue was purified by flash chromatography

出典と根拠

ORDレコード
ord-5c815a5d76614fe789dcfaa6924e0a9a
出典データセット
uspto-grants-2016_03
特許番号
US09296758B2

反応ノート

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