Morpholine → HCID 123464039, compound
Reaction equation
[Cl:1][C:2]1[CH:16]=[CH:15][C:5]([O:6][CH2:7][C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])=[C:4]([C:17]2[C:18]([CH3:27])=[N:19][C:20](S(C)(=O)=O)=[N:21][CH:22]=2)[CH:3]=1.[NH:28]1[CH2:33][CH2:32][O:31][CH2:30][CH2:29]1>O1CCOCC1>[C:11]([O:10][C:8](=[O:9])[CH2:7][O:6][C:5]1[CH:15]=[CH:16][C:2]([Cl:1])=[CH:3][C:4]=1[C:17]1[C:18]([CH3:27])=[N:19][C:20]([N:28]2[CH2:33][CH2:32][O:31][CH2:30][CH2:29]2)=[N:21][CH:22]=1)([CH3:14])([CH3:13])[CH3:12]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of the product from step (vii) (0.15 g) and morpholine (0.15 ml) in dioxane (3 ml) was heated at 90° C. for 24 h, cooled and the solvent evaporated under reduced pressure.
Workup
- temperaturecooled
- customthe solvent evaporated under reduced pressure
Sources & evidence
- ORD record
- ord-7df58ce931af4eaf8d3943363166f333
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08158820B2
Reaction notes
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