N4-(3-isopropoxypropyl)-3-nitro[1,5]naphthyridin-4-amine → N4-(3-isopropoxypropyl)[1,5]naphthyridine-3,4-diamine

HRID 47494Notes

Reaction equation

HRID 47494 reaction equation
[CH:1]([O:4][CH2:5][CH2:6][CH2:7][NH:8][C:9]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][N:17]=2)[N:12]=[CH:11][C:10]=1[N+:19]([O-])=O)([CH3:3])[CH3:2]>[Pt].C(OCC)(=O)C>[CH:1]([O:4][CH2:5][CH2:6][CH2:7][NH:8][C:9]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][N:17]=2)[N:12]=[CH:11][C:10]=1[NH2:19])([CH3:3])[CH3:2]

Participants

4

Reactant 1

HCID 54329107N4-(3-isopropoxypropyl)-3-nitro[1,5]naphthyridin-4-amine

Product 1

HCID 54100366N4-(3-isopropoxypropyl)[1,5]naphthyridine-3,4-diamineYield 95.4%

Reagents, catalysts & solvents 2

HCID 23939PlatinumCatalystHCID 8857Ethyl AcetateSolvent

Procedure

N4-(3-Isopropoxypropyl)-3-nitro[1,5]naphthyridin-4-amine (4.2 g, 14.5 mmol), platinum on carbon (1.1 g of 5%), and ethyl acetate (100 mL) were placed in a hydrogenation flask. The mixture was shaken under a hydrogen pressure of 50 psi (3.5 Kg/cm2) for 2.5 hours. The reaction mixture was filtered and the catalyst was washed with ethyl acetate. The filtrate was dried over magnesium sulfate, filtered and then concentrated under vacuum to provide 3.6 g of N4-(3-isopropoxypropyl)[1,5]naphthyridine-3,4-diamine as a bright yellow oil. 1H NMR (300 MHz, CDCl3): δ8.70 (dd, J=4.1,1.6 Hz, 1H), 8.39 (s, 1H), 8.17 (dd, J=8.4,1.6 Hz, 1H), 7.37 (dd, J=8.4, 4.1 Hz, 1H), 5.99 (broad s, 1H), 3.98 (broad s, 2H), 3.63-3.55 (m, 5H), 1.87 (pentet, J=6.2 Hz, 2H), 1.17 (d, J=6.1 Hz, 6H); MS (EI): m/e 260.1630 (260.1637 calc'd for C14H20N4O).

Workup

  1. filtrationThe reaction mixture was filtered
  2. washthe catalyst was washed with ethyl acetate
  3. dry with materialThe filtrate was dried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated under vacuum

Sources & evidence

ORD record
ord-7ca9569735314eaabc0419b4f694f8e4
Source dataset
uspto-grants-2004_03
Patent number
US06699878B2

Reaction notes

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