(1-Methyl-1H-pyrazol-5-yl)methanamine → HCID 67434135, compound
Reaction equation
[Si]([O:18][CH2:19][C:20]1[C:21]([N:35]2[CH2:40][C@H:39]([CH3:41])[O:38][C@H:37]([CH3:42])[CH2:36]2)=[C:22]([F:34])[C:23]2[O:27][N:26]=[C:25]([C:28]([O:30]CC)=O)[C:24]=2[CH:33]=1)(C(C)(C)C)(C1C=CC=CC=1)C1C=CC=CC=1.[CH3:43][N:44]1[C:48]([CH2:49][NH2:50])=[CH:47][CH:46]=[N:45]1>>[CH3:41][C@@H:39]1[CH2:40][N:35]([C:21]2[C:20]([CH2:19][OH:18])=[CH:33][C:24]3[C:25]([C:28]([NH:50][CH2:49][C:48]4[N:44]([CH3:43])[N:45]=[CH:46][CH:47]=4)=[O:30])=[N:26][O:27][C:23]=3[C:22]=2[F:34])[CH2:36][C@H:37]([CH3:42])[O:38]1Participants
3
Procedure
Starting materials: ethyl 5-((tert-butyldiphenylsilyloxy)methyl)-6-((2R,6S)-2,6-dimethylmorpholino)-7-fluorobenzo[d]isoxazole-3-carboxylate (Intermediate 204) and (1-methyl-1H-pyrazol-5-yl)methanamine
Sources & evidence
- ORD record
- ord-acd323e9b297470bb3392e543e7a8ff1
- Source dataset
- uspto-grants-2014_02
- Patent number
- US08658641B2
Reaction notes
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