3-Fluorobenzoic Acid → 3-fluorobenzoic acid N'-{(E)-3-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]acryloyl}hydrazide

HRID 599553Notes

Reaction equation

HRID 599553 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]1

Participants

9

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 is as follows.

Workup

  1. filtrationthe precipitated solid was collected by filtration

Sources & evidence

ORD record
ord-048b9f0f77734a629f7d1e00d84d6888
Source dataset
uspto-grants-2011_03
Patent number
US07897632B2

Reaction notes

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