3,5-Dimethylisoxazole-4-isocyanate → 2-(4-{4-[3-(3,5-Dimethyl-isoxazol-4-yl)-ureido]-2-fluoro-phenyl}-piperazin-1-yl)-N,N-diethyl-2-phenyl-acetamide

HRID 1927595Notes

Reaction equation

HRID 1927595 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:13][CH2:12][N:11]([CH:14]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[C:15]([N:17]([CH2:20][CH3:21])[CH2:18][CH3:19])=[O:16])[CH2:10][CH2:9]2)=[C:4]([F:28])[CH:3]=1.[N:29]([C:32]1[C:33]([CH3:38])=[N:34][O:35][C:36]=1[CH3:37])=[C:30]=[O:31]>ClCCCl>[CH3:38][C:33]1[C:32]([NH:29][C:30](=[O:31])[NH:1][C:2]2[CH:7]=[CH:6][C:5]([N:8]3[CH2:13][CH2:12][N:11]([CH:14]([C:22]4[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=4)[C:15]([N:17]([CH2:18][CH3:19])[CH2:20][CH3:21])=[O:16])[CH2:10][CH2:9]3)=[C:4]([F:28])[CH:3]=2)=[C:36]([CH3:37])[O:35][N:34]=1

Participants

4

Procedure

A mixture of 2-[4-(4-amino-2-fluoro-phenyl)-piperazin-1-yl]-N,N-diethyl-2-phenyl-acetamide (0.30 mmol) and 4-isocyanato-3,5-dimethyl-isoxazole (1.0 mmol) in DCE (10 mL) was stirred at rt for 16 h. The solid that had formed was collected by filtration and dried under vacuum to give the title compound (100 mg, 64%). MS (ESI): mass calcd. for C28H35FN6O3, 522.28. m/z found, 523.4 [M+H]+. 1H NMR (CDCl3): 8.60-8.40 (br s, 1H), 7.60-7.25 (m, 6H), 6.78-6.71 (m, 1H), 6.68-6.57 (m, 1H), 4.21 (s, 1H), 3.60-3.40 (m, 2H), 3.39-3.15 (m, 2H), 2.95-2.45 (m, 8H), 2.24 (s, 3H), 2.13 (s, 3H), 1.11 (t, J=7.1, 3H), 1.05 (t, J=7.1, 3H).

Workup

  1. customThe solid that had formed
  2. filtrationwas collected by filtration
  3. customdried under vacuum

Sources & evidence

ORD record
ord-f70c43f864df4fa0915b8b13d984bbc3
Source dataset
uspto-grants-2012_05
Patent number
US08183239B2

Reaction notes

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