Dimethylformamide → HCID 22057962, compound
Reaction equation
C(N(C(C)C)CC)(C)C.O1C[CH2:14][N:13]([C:16]2[CH:17]=[C:18]([CH:22]=[CH:23][CH:24]=2)[C:19]([OH:21])=O)[CH2:12]C1.[NH2:25][C:26]1[CH:27]=[CH:28][C:29]([CH3:45])=[C:30]([NH:32][C:33]([C:35]2[CH:36]=[C:37]3[C:42](=[CH:43][CH:44]=2)[N:41]=[CH:40][CH:39]=[CH:38]3)=[O:34])[CH:31]=1.CN(C=O)C>O>[CH3:14][N:13]([CH3:12])[C:16]1[CH:17]=[C:18]([CH:22]=[CH:23][CH:24]=1)[C:19]([NH:25][C:26]1[CH:27]=[CH:28][C:29]([CH3:45])=[C:30]([NH:32][C:33]([C:35]2[CH:36]=[C:37]3[C:42](=[CH:43][CH:44]=2)[N:41]=[CH:40][CH:39]=[CH:38]3)=[O:34])[CH:31]=1)=[O:21]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Diisopropylethylamine (0.174 ml) was added to a stirred mixture of 3-morpholinobenzoic acid (0.104 g), N-(5-amino-2-methylphenyl)quinoline-6-carboxamide (0.14 g), 2-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate(V) (0.23 g) and DMF (1 ml) and the resultant mixture was stirred at ambient temperature for 16 hours. The reaction mixture was poured into water and the resultant solid was isolated, washed with a saturated aqueous sodium bicarbonate solution and dried in a vacuum oven. There was thus obtained the title compound (0.216 g); NMR Spectrum: (DMSOd6) 2.25 (s, 3H), 3.18 (m, 4H), 3.75 (m, 4H), 7.14 (d, 1H), 7.25 (d, 1H), 7.36 (m, 2H), 7.44 (s, 1H), 7.62 (m, 2H), 7.86 (s, 1H), 8.13 (d, 1H), 8.28 (d, 1H), 8.52 (d, 1H), 8.65 (s, 1H), 9.0 (s, 1H), 10.14 (m, 2H); Mass Spectrum: M+H+ 467.
Workup
- customthe resultant solid was isolated
- washwashed with a saturated aqueous sodium bicarbonate solution
- customdried in a vacuum oven
Sources & evidence
- ORD record
- ord-76137cc5f3ca4adeb543fae73cb6b64d
- Source dataset
- uspto-grants-2006_06
- Patent number
- US07060700B2
Reaction notes
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