3-Cyano-5-isopentylpyridine → methyl 3-(aminomethyl)-5-(N-methylmethylsulfonamido)benzoate
Reaction equation
[N:1]([CH2:4][C:5]1[CH:6]=[C:7]([CH:12]=[C:13]([N:15]([CH3:20])[S:16]([CH3:19])(=[O:18])=[O:17])[CH:14]=1)[C:8]([O:10][CH3:11])=[O:9])=[N+]=[N-].C(C1C=NC=C(CCC(C)C)C=1)#N>>[NH2:1][CH2:4][C:5]1[CH:6]=[C:7]([CH:12]=[C:13]([N:15]([CH3:20])[S:16]([CH3:19])(=[O:18])=[O:17])[CH:14]=1)[C:8]([O:10][CH3:11])=[O:9]Participants
3
Procedure
The desired product was synthesized from methyl 3-(azidomethyl)-5-(N-methylmethylsulfonamido)benzoate following the general procedure as described for 3-cyano-5-isopentylpyridine.
Sources & evidence
- ORD record
- ord-4afc6510d58046ec8d8e36eb111148e2
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08299267B2
Reaction notes
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