Morpholine → HCID 68478808, compound
Reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([NH:11][CH2:12][CH:13]3[CH2:18][CH2:17][O:16][CH2:15][CH2:14]3)[CH:10]=1)[NH:7][C:6]([C:19]1[S:20][CH2:21][C@@H:22]([CH2:24][CH2:25]O)[N:23]=1)=[CH:5]2.[NH:27]1[CH2:32][CH2:31][O:30][CH2:29][CH2:28]1>>[CH3:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([NH:11][CH2:12][CH:13]3[CH2:14][CH2:15][O:16][CH2:17][CH2:18]3)[CH:10]=1)[NH:7][C:6]([C:19]1[S:20][CH2:21][C@H:22]([CH2:24][CH2:25][N:27]3[CH2:32][CH2:31][O:30][CH2:29][CH2:28]3)[N:23]=1)=[CH:5]2Participants
3
Procedure
2-((R)-2-{5-methyl-7-[(tetrahydro-pyran-4-ylmethyl)-amino]-1H-indol-2-yl}-4,5-dihydro-thiazol-4-yl)-ethanol prepared in Step B and morpholine were reacted according to the same procedure as Example 156 to give the title compound.
Sources & evidence
- ORD record
- ord-86871643ccbc4a7a93c5f22871620a6f
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08889691B2
Reaction notes
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