Morpholine → HCID 67094356, compound
Reaction equation
C([O:4][C:5]1[CH:13]=[C:12]2[C:8]([C:9](=[O:21])[N:10]([C:14]3[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][CH:15]=3)[CH2:11]2)=[CH:7][C:6]=1[O:22][C:23](=[O:25])[CH3:24])(=O)C.N1CCOCC1>CN(C)C=O>[Cl:20][C:17]1[CH:16]=[CH:15][C:14]([N:10]2[C:9](=[O:21])[C:8]3[C:12](=[CH:13][C:5]([OH:4])=[C:6]([O:22][C:23](=[O:25])[CH3:24])[CH:7]=3)[CH2:11]2)=[CH:19][CH:18]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of acetic acid 6-acetoxy-2-(4-chloro-phenyl)-3-oxo-2,3-dihydro-1H-isoindol-5-yl ester (0.5 g) in dry N,N-dimethylformamide (15 ml) was treated with morpholine (0.13 ml) at 0-5° C. and stirred then for an hour at room temperature. The reaction was poured into ice water and filtered.
Workup
- waitfor an hour at room temperature
- filtrationfiltered
Sources & evidence
- ORD record
- ord-46e8a9b686624383bc1cf6f0b75d059a
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08318785B2
Reaction notes
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