Morpholine → [3,5-Difluoro-4-(4-methoxy-benzylamino)-phenyl]-morpholin-4-yl-methanone
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([F:21])[C:10]=1[NH:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[CH:15][CH:14]=1)[C:5]([OH:7])=O.[NH:22]1[CH2:27][CH2:26][O:25][CH2:24][CH2:23]1>>[F:21][C:9]1[CH:8]=[C:4]([C:5]([N:22]2[CH2:27][CH2:26][O:25][CH2:24][CH2:23]2)=[O:7])[CH:3]=[C:2]([F:1])[C:10]=1[NH:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[CH:15][CH:14]=1Participants
3
Procedure
Using 3,5-difluoro-4-(4-methoxy-benzylamino)-benzoic acid (95.4 mg) obtained in Step B in Example 1-D-24 and morpholine (33.8 μl) instead of 1-ethyl-piperazine, in the same manner as Step C in Example 1-D-24, the desired compound was obtained as a crude product (111 mg, 94%).
Sources & evidence
- ORD record
- ord-9ddcad69ceb94f2e8828ebcf9f0f0bd5
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08022205B2
Reaction notes
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