ethyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylate → HCID 59569900, compound
Reaction equation
[N:1]([CH2:4][C:5]1[CH:6]=[N:7][N:8]([C:11]([CH3:14])([CH3:13])[CH3:12])[C:9]=1[CH3:10])=[N+]=[N-].C(N1C(C)=C(C(OCC)=O)C=N1)(C)(C)C>>[C:11]([N:8]1[C:9]([CH3:10])=[C:5]([CH2:4][NH2:1])[CH:6]=[N:7]1)([CH3:14])([CH3:13])[CH3:12]Participants
3
Procedure
4-(azidomethyl)-1-tert-butyl-5-methyl-1H-pyrazole was generated from ethyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylate according to a procedure similar to that described for the 2,6 dimethyl 3,5-pyridyl derivative, then reduced to the crude primary amine, following procedures described herein.
Sources & evidence
- ORD record
- ord-b46bc853faa6455a8f113a899461a030
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08299267B2
Reaction notes
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