Benzenamine, 4-(4-morpholinyl)- → HCID 86587185, compound

HRID 1795338Notes

Reaction equation

HRID 1795338 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([O:16][CH3:17])[CH:5]=[C:6]2[C:11]=1[NH:10][C:9]([C:12]([OH:14])=O)=[CH:8][C:7]2=[O:15].CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.C1C=CC2N(O)N=NC=2C=1.[O:50]1[CH2:55][CH2:54][N:53]([C:56]2[CH:62]=[CH:61][C:59]([NH2:60])=[CH:58][CH:57]=2)[CH2:52][CH2:51]1.C(N(C(C)C)CC)(C)C>CN(C)C=O>[N:53]1([C:56]2[CH:57]=[CH:58][C:59]([NH:60][C:12]([C:9]3[NH:10][C:11]4[C:6]([C:7](=[O:15])[CH:8]=3)=[CH:5][C:4]([O:16][CH3:17])=[CH:3][C:2]=4[Br:1])=[O:14])=[CH:61][CH:62]=2)[CH2:52][CH2:51][O:50][CH2:55][CH2:54]1

Participants

7

Reactant 5

HCID 75655Benzenamine, 4-(4-morpholinyl)-HCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 2733207O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 22142213HCID 22142213, compound

Product 1

HCID 86587185HCID 86587185, compoundYield 58.3%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

To a yellow suspension of 8-bromo-6-methoxyoxo-1,4-dihydro-quinoline-2-carboxylic acid (Reference Example 27a) (3.446 g, 11.56 mmol), TBTU (9.039 g, 28.15 mmol), and HOBt (3.757 g, 27.8 mmol) in 100 mL dimethylformamide was added 4-morpholinoaniline (2.733 g, 15.3 mmol) and diisopropylethyl amine (8.2 mL, 50.2 mmol). The resulting marroon solution was stirred at room temperature under nitrogen for 16 hours during which time the reaction became greenish brown and formed a large amount of precipitate. The reaction mixture was filtered and the solids washed with dimethylformamide, water, and methanol; Drying under high vacuum afforded the desired product as a yellow solid (3.09 g, 58%). 1H NMR (300 MHz, DMSO, d6) δ 12.13 (s, 1 H, NH), 10.18 (s, 1 H, C(O)NH), 7.90 (d, 1 H, Jm=2.7 Hz, ArH5), 7.68 (d, 2 H, Jo=9.0 Hz, ArH2′ & H6′), 7.63 (s, 1 H, C═CH), 7.51 (d, 1 H, Jm=2.7 Hz, ArH7), 7.00 (d, 2 H, Jo=9.0 Hz, ArH3′ & H5′), 3.94 (s, 3 H, OCH3), 3.75 (t, 4 H, J=4.8 Hz, OCH2CH2N), 3.10 (t, 4 H, J=4.8 Hz, OCH2CH2N); Mass Spec.: calc. for [C21H20BrN3O4+H]+ Theor. m/z=458, 460; Obs.=458, 460.

Workup

  1. customformed a large amount of precipitate
  2. filtrationThe reaction mixture was filtered
  3. washthe solids washed with dimethylformamide, water, and methanol
  4. customDrying under high vacuum

Sources & evidence

ORD record
ord-76b66d105aa946489d034891137f5a6e
Source dataset
uspto-grants-2006_04
Patent number
US07026314B2

Reaction notes

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