3-Fluorobenzoic Acid → 3-fluorobenzoic acid N'-{(E)-3-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]acryloyl}hydrazide
Reaction equation
C1C=CC2N(O)N=NC=2C=1.Cl.Cl.[CH3:13][O:14][C:15]1[CH:16]=[C:17](/[CH:27]=[CH:28]/[C:29]([NH:31][NH2:32])=[O:30])[CH:18]=[CH:19][C:20]=1[N:21]1[CH:25]=[C:24]([CH3:26])[N:23]=[CH:22]1.[F:33][C:34]1[CH:35]=[C:36]([CH:40]=[CH:41][CH:42]=1)[C:37](O)=[O:38].C(N(C(C)C)CC)(C)C>CN(C=O)C.O.C(OCC)(=O)C.C(Cl)CCl>[CH3:13][O:14][C:15]1[CH:16]=[C:17](/[CH:27]=[CH:28]/[C:29]([NH:31][NH:32][C:37](=[O:38])[C:36]2[CH:40]=[CH:41][CH:42]=[C:34]([F:33])[CH:35]=2)=[O:30])[CH:18]=[CH:19][C:20]=1[N:21]1[CH:25]=[C:24]([CH3:26])[N:23]=[CH:22]1Participants
9
Reactant 4
Product 1
Reagents, catalysts & solvents 4
Procedure
HOBT (70 mg) and EDC (100 mg) were added to a solution of (E)-3-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]acrylic acid hydrazide dihydrochloride (120 mg), 3-fluorobenzoic acid (49 mg) and IPEA (0.37 mL) in DMF, and the reaction solution was stirred at room temperature for 12 hours. Ethyl acetate and water were added to the reaction solution, and the precipitated solid was collected by filtration to obtain 86 mg of the title compound. The property value of the compound as follows.
Workup
- filtrationthe precipitated solid was collected by filtration
Sources & evidence
- ORD record
- ord-33613682ef374bf89412acb60a6713c2
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07713993B2
Reaction notes
Loading…