Morpholine → HCID 58442372, compound
Reaction equation
Cl[C:2]1[N:7]=[C:6]([N:8]2[C:12]([CH3:13])=[CH:11][C:10]([CH3:14])=[N:9]2)[N:5]=[C:4]([NH:15][CH:16]2[CH2:24][C:23]3[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=3)[CH2:17]2)[CH:3]=1.[NH:25]1[CH2:30][CH2:29][O:28][CH2:27][CH2:26]1>>[CH3:14][C:10]1[CH:11]=[C:12]([CH3:13])[N:8]([C:6]2[N:5]=[C:4]([NH:15][CH:16]3[CH2:24][C:23]4[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=4)[CH2:17]3)[CH:3]=[C:2]([N:25]3[CH2:30][CH2:29][O:28][CH2:27][CH2:26]3)[N:7]=2)[N:9]=1Participants
3
Procedure
Was prepared according to example 4 from [6-chloro-2-(3,5-dimethyl-pyrazol-1-yl)-pyrimidin-4-yl]-indan-2-yl-amine and morpholine. Mp. 66-70° C.
Workup
- customWas prepared
Sources & evidence
- ORD record
- ord-5b115e8a595f41508c65a0538e309f78
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08618099B2
Reaction notes
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