Water → N'-hydroxy-4-(6-methoxyquinolin-2-yl)benzenecarboximidamide

HRID 1410584Notes

Reaction equation

HRID 1410584 reaction equation
CO[C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]=[C:8]([C:13]1[CH:20]=[CH:19][C:16]([C:17]#[N:18])=[CH:15][CH:14]=1)[CH:7]=[CH:6]2.Cl.[NH2:22][OH:23].[C:24]([O-])([O-])=O.[K+].[K+].[OH2:30]>CO>[OH:23][NH:22][C:17](=[NH:18])[C:16]1[CH:19]=[CH:20][C:13]([C:8]2[CH:7]=[CH:6][C:5]3[C:10](=[CH:11][CH:12]=[C:3]([O:30][CH3:24])[CH:4]=3)[N:9]=2)=[CH:14][CH:15]=1

Participants

6

Reactant 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 443297Hydroxyamine hydrochlorideHCID 621350HCID 621350, compound

Product 1

HCID 178487828N'-hydroxy-4-(6-methoxyquinolin-2-yl)benzenecarboximidamide

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Scheme 4, route B, step 1: 4-(6-methoxyquinolin-2-yl)benzonitrile (prepared via scheme 3) (780 mg, 3.00 mmol) was suspended in methanol (10 mL) and hydroxylamine hydrochloride (639 mg, 10.7 mmol), K2CO3 (414 mg, 3.00 mmol) were added. The reaction mixture was refluxed for 12 hours. Water (15 mL) was added and the precipitated solid was collected by filtration, washed with ethanol (5 mL) and dried over high vacuum to give the product (600 mg).

Workup

  1. temperatureThe reaction mixture was refluxed for 12 hours
  2. filtrationthe precipitated solid was collected by filtration
  3. washwashed with ethanol (5 mL)
  4. customdried over high vacuum

Sources & evidence

ORD record
ord-16edf0ce70fc4d9e82bcefb6b0f2d579
Source dataset
uspto-grants-2014_12
Patent number
US08921562B2

Reaction notes

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