Dimethylformamide → HCID 22057962, compound

HRID 1828748Notes

Reaction equation

HRID 1828748 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

6

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

  1. customthe resultant solid was isolated
  2. washwashed with a saturated aqueous sodium bicarbonate solution
  3. customdried in a vacuum oven

Sources & evidence

ORD record
ord-76137cc5f3ca4adeb543fae73cb6b64d
Source dataset
uspto-grants-2006_06
Patent number
US07060700B2

Reaction notes

Loading…