Dimethylformamide → HCID 66749947, compound

HRID 1405663Notes

Reaction equation

HRID 1405663 reaction equation
[CH:1]1[CH:2]=[CH:3][C:4]2N(O)N=[N:7][C:5]=2C=1.CC[N:13]=[C:14]=[N:15]CCCN(C)C.Cl.[CH:23]([C:26]1[CH:34]=[CH:33][C:29]([C:30]([OH:32])=O)=[CH:28][CH:27]=1)([CH3:25])[CH3:24].C(=O)([O-])O.[Na+].C[N:41](C=O)C>O>[CH3:25][CH:23]([C:26]1[CH:27]=[CH:28][C:29]([C:30]2[O:32][N:15]=[C:14]([C:4]3[C:5]([NH2:7])=[N:41][CH:1]=[CH:2][CH:3]=3)[N:13]=2)=[CH:33][CH:34]=1)[CH3:24]

Participants

7

Procedure

A mixture of 2-amino-N′-hydroxypyridine-3-carboxyamide (1070 mg), HOBt.H2O (1185 mg), EDCI HCl (1483 mg) and 4-isopropylbenzoic acid (1270 mg) in dehydrated DMF (40 mL) was stirred at room temperature overnight and at 80° C. for 24 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (302 mg) as a white solid.

Workup

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified by silica gel column chromatography (ethyl acetate/hexane)

Sources & evidence

ORD record
ord-e4804df8ec414c37982f771d294946ad
Source dataset
uspto-grants-2014_12
Patent number
US08916551B2

Reaction notes

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