HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014364Generated: October 25, 2026
N,N-dimethyl-3-[6-(methyloxy)-7-nitro-3,4-dihydro-1(2H)-quinolinyl]-3-oxo-1-propanamine → 1-[3-(Dimethylamino)propanoyl]-6-(methyloxy)-1,2,3,4-tetrahydro-7-quinolinamine
https://huagongshe.com/reaction/1014364
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-dimethyl-3-[6-(methyloxy)-7-nitro-3,4-dihydro-1(2H)-quinolinyl]-3-oxo-1-propanamine | HCID 59442063 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-[3-(Dimethylamino)propanoyl]-6-(methyloxy)-1,2,3,4-tetrahydro-7-quinolinamine | HCID 59442002 | 95.1% |
Reaction Steps
N,N-dimethyl-3-[6-(methyloxy)-7-nitro-3,4-dihydro-1(2H)-quinolinyl]-3-oxo-1-propanamine (crude from previous reaction, assumed 0.91 mmol) was dissolved in methanol (10 mL), treated with 10% palladium on carbon (50 mg, Aldrich), and stirred under 60 psi of hydrogen pressure for 16 h in a Fischer-Porter apparatus. The pressure was released, the reaction vessel evacuated, and back-filled with nitrogen twice. The mixture was filtered through celite and the filtrate was concentrated to provide 1-[3-(dimethylamino)propanoyl]-6-(methyloxy)-1,2,3,4-tetrahydro-7-quinolinamine (0.24 g, 93% over three steps). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.74-1.85 (m, 2 H), 2.09 (bs, 6 H), 2.51-2.60 (m, some signals may be underneath DMSO, 6 H), 3.58 (t, J=6.4 Hz, 2 H), 3.74 (s, 3 H), 4.60 (bs, 2 H), 6.60 (s, broadening due to amide rotomers, 2 H); ESIMS (M+H)+=278.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981903B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-3893f31864c248778ebb42b4beb4f39a |
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| Source note | uspto-grants-2011_07 |
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