Potassium Carbonate → HCID 86746854, compound

HRID 1769207Notes

Reaction equation

HRID 1769207 reaction equation
[CH2:1]1[O:19][C:4]([CH2:17][CH3:18])([CH2:5][C:6]2[CH:11]=[CH:10][CH:9]=[C:8]([C:12]([O:14][CH3:15])=[O:13])[C:7]=2[NH2:16])[O:3][CH2:2]1.[C:20]([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=1[C:28]1[CH:33]=[CH:32][C:31]([CH2:34]Br)=[CH:30][CH:29]=1)#[N:21].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O.C(OCC)(=O)C>[CH2:2]1[O:3][C:4]([CH2:17][CH3:18])([CH2:5][C:6]2[CH:11]=[CH:10][CH:9]=[C:8]([C:12]([O:14][CH3:15])=[O:13])[C:7]=2[NH:16][CH2:34][C:31]2[CH:30]=[CH:29][C:28]([C:23]3[CH:24]=[CH:25][CH:26]=[CH:27][C:22]=3[C:20]#[N:21])=[CH:33][CH:32]=2)[O:19][CH2:1]1

Participants

6

Procedure

A mixture of 1-(2-amino-3-methoxycarbonylphenyl)butan-2-one ethylene ketal (37) (0.7 g) (prepared, e.g., as described in Preparation 25), 2'-(cyano)biphenyl-4-yl-methylbromide (0.826 g) and potassium carbonate (0.41 g) in dimethylformamide (20 ml) was heated at 80°-90° C. for 16 hours under an inert atmosphere. The reaction mixture was concentrated under reduced pressure, and the residue obtained was diluted with ethyl acetate (100 ml), washed twice with cold water, and then brine. The solvent was removed under reduced pressure and the residue was chromatographed on silica gel, eluting with 20% ethyl acetate/hexane, to give 1-[2-(2"-cyanobiphenyl-4'-ylmethylamino)-3-methoxycarbonylphenyl]butan-2-one ethylene ketal (0.52 g), a compound of Formula (38), as an oil.

Workup

  1. temperaturewas heated at 80°-90° C. for 16 hours under an inert atmosphere
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. customthe residue obtained
  4. washwashed twice with cold water
  5. customThe solvent was removed under reduced pressure
  6. customthe residue was chromatographed on silica gel
  7. washeluting with 20% ethyl acetate/hexane

Sources & evidence

ORD record
ord-0a4ca3172a80458ebe36f6337b63c8a2
Source dataset
uspto-grants-1995_01
Patent number
US05380739

Reaction notes

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