2-(Chloromethyl)-3-methylpyridine → 3-(Methoxymethoxy)-1-(methoxymethyl)-5-([(3-methylpyridin-2-yl)methyl]sulfanyl)pyridin-2(1H)-one
Reaction equation
C(C1C=CC(C[S:8][C:9]2[CH:10]=[C:11]([O:19][CH2:20][O:21][CH3:22])[C:12](=[O:18])[N:13]([CH2:15][O:16][CH3:17])[CH:14]=2)=CC=1)C.Cl[CH2:26][C:27]1[C:32]([CH3:33])=[CH:31][CH:30]=[CH:29][N:28]=1>>[CH3:22][O:21][CH2:20][O:19][C:11]1[C:12](=[O:18])[N:13]([CH2:15][O:16][CH3:17])[CH:14]=[C:9]([S:8][CH2:26][C:27]2[C:32]([CH3:33])=[CH:31][CH:30]=[CH:29][N:28]=2)[CH:10]=1Participants
3
Procedure
Prepared as described for 5-[(4-ethylbenzyl)sulfanyl]-3-(methoxymethoxy)-1-(methoxymethyl)pyridin-2(1H)-one (Intermediate 17) but using 2-(chloromethyl)-3-methylpyridine instead of 1-(chloromethyl)-4-ethylbenzene.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-628c60e1a3c34792939273b1e5e89b39
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09180122B2
Reaction notes
Loading…