Morpholine → HCID 15388686, compound
Reaction equation
[NH:1]1[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[CH2:7]([N:14]1[C:18]2[CH:19]=[C:20]([O:23][CH2:24][CH2:25][CH2:26]Cl)[CH:21]=[CH:22][C:17]=2[N:16]=[C:15]1[C:28]1[CH:33]=[CH:32][CH:31]=[C:30]([CH3:34])[CH:29]=1)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.C(C1C=CC=CC=1N(C(C)C)CC)(C)C>C(#N)C>[CH2:7]([N:14]1[C:18]2[CH:19]=[C:20]([O:23][CH2:24][CH2:25][CH2:26][N:1]3[CH2:6][CH2:5][O:4][CH2:3][CH2:2]3)[CH:21]=[CH:22][C:17]=2[N:16]=[C:15]1[C:28]1[CH:33]=[CH:32][CH:31]=[C:30]([CH3:34])[CH:29]=1)[C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared by first adding morpholine (1.02 g, 11.77 mmol) and the compound of Example 97, supra, (0.39 g, 1.00 mmol) to 125 ml of acetonitrile while stirring under nitrogen purge. To this mixture is then added diisopropylethyl aniline (1.51 ml, 8.67 mmol) dropwise. This reaction mixture is then allowed to stir overnight.
Workup
- custompurge
Sources & evidence
- ORD record
- ord-520e454afca0463e89bedb29367d56ea
- Source dataset
- uspto-grants-2000_02
- Patent number
- US06030992
Reaction notes
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