Morpholine → HCID 44187165, compound
Reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([NH:11][CH:12]3[CH2:17][CH2:16][O:15][CH2:14][CH2:13]3)[CH:10]=1)[NH:7][C:6]([C:18]1[O:19][CH2:20][C@@H:21]([CH:23](O)[CH3:24])[N:22]=1)=[CH:5]2.[NH:26]1[CH2:31][CH2:30][O:29][CH2:28][CH2:27]1>>[CH3:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([NH:11][CH:12]3[CH2:17][CH2:16][O:15][CH2:14][CH2:13]3)[CH:10]=1)[NH:7][C:6]([C:18]1[O:19][CH2:20][C@H:21]([CH2:23][CH2:24][N:26]3[CH2:31][CH2:30][O:29][CH2:28][CH2:27]3)[N:22]=1)=[CH:5]2Participants
3
Procedure
The compound obtained in Example 104 and morpholine were reacted according to the procedures as Preparation 33 and Example 15 in the order to give the title compound.
Workup
- customaccording to the procedures as Preparation 33 and Example 15 in the order
Sources & evidence
- ORD record
- ord-0be4cd9475574da9914ac335898779c4
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08349885B2
Reaction notes
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