2-Amino-5-cyanopyridine → Phenyl (5-cyanopyridin-2-yl)carbamate
Reaction equation
NC1C=CC(C#N)=CN=1.[C:10]1([O:16][C:17](=[O:32])[NH:18][C:19]2[CH:24]=[C:23](OCCOC)[C:22]([C:30]#[N:31])=[CH:21][N:20]=2)[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>>[C:10]1([O:16][C:17](=[O:32])[NH:18][C:19]2[CH:24]=[CH:23][C:22]([C:30]#[N:31])=[CH:21][N:20]=2)[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1Participants
3
Procedure
From 2-amino-5-cyanopyridine, reacted in an analogous manner to the preparation of intermediate 108. (UPLC-MS 6) tR 0.92; ESI-MS 240.1 [M+H]+.
Sources & evidence
- ORD record
- ord-7c1bceba99d94614a9c13100d9243a4d
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09266883B2
Reaction notes
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