2-fluoro-5-methoxy-N-(1-methylpiperidin-4-yl)-4-nitrobenzamide → 4-amino-2-fluoro-5-methoxy-N-(1-methylpiperidin-4-yl)benzamide

HRID 2234357

Reaction equation

HRID 2234357 reaction equation
[F:1][C:2]1[CH:17]=[C:16]([N+:18]([O-])=O)[C:15]([O:21][CH3:22])=[CH:14][C:3]=1[C:4]([NH:6][CH:7]1[CH2:12][CH2:11][N:10]([CH3:13])[CH2:9][CH2:8]1)=[O:5]>[Pd].CO>[NH2:18][C:16]1[C:15]([O:21][CH3:22])=[CH:14][C:3]([C:4]([NH:6][CH:7]2[CH2:12][CH2:11][N:10]([CH3:13])[CH2:9][CH2:8]2)=[O:5])=[C:2]([F:1])[CH:17]=1

Participants

4

Reactant 1

HCID 671177462-fluoro-5-methoxy-N-(1-methylpiperidin-4-yl)-4-nitrobenzamide

Product 1

HCID 669272854-amino-2-fluoro-5-methoxy-N-(1-methylpiperidin-4-yl)benzamide

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 887MethanolSolvent

Conditions

Temperature
25 °C

Procedure

2-fluoro-5-methoxy-N-(1-methyl-4-piperidyl)-4-nitro-benzamide Intermediate 28; 1.3 g, 4.2 mmol) 10% Palladium on Carbon (100 mg) and Methanol (50 mL) were combined and stirred at 25° C. under Hydrogen at 1 bar pressure for 18 hours.

Sources & evidence

ORD record
ord-9ecb695237ea4969af047f347a4c79bc
Source dataset
uspto-grants-2010_05
Patent number
US07709471B2

Linked notes

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