Morpholine → 4-Chloro-N-(5-cyclopropyl-1H-pyrazol-3-yl)-6-morpholino-1,3,5-triazin-2-amine
Reaction equation
ClC1N=C(Cl)N=C(NC2NN=C(C3CC3)C=2)N=1.N1CCOCC1.[Cl:24][C:25]1[N:30]=[C:29]([NH:31][C:32]2[NH:36][N:35]=[C:34]([CH:37]3[CH2:39][CH2:38]3)[CH:33]=2)[N:28]=[C:27]([N:40]2[CH2:44][CH2:43]C[C@@:41]2(C)[C:45](NC2C=NC(F)=CC=2)=[O:46])[N:26]=1>>[Cl:24][C:25]1[N:26]=[C:27]([N:40]2[CH2:44][CH2:43][O:46][CH2:45][CH2:41]2)[N:28]=[C:29]([NH:31][C:32]2[CH:33]=[C:34]([CH:37]3[CH2:39][CH2:38]3)[NH:35][N:36]=2)[N:30]=1Participants
4
Procedure
Compound 112A was prepared from 1A and morpholine as described for 1C. LC/MS [M+H]+: 322/324; Ret time (Method F): 2.81 min.
Workup
- custom2.81 min.
Sources & evidence
- ORD record
- ord-307f7e109b6847dc81ded23e0eb5ccb8
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08415340B2
Reaction notes
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