5-Chloro-2-(chloromethyl)pyridine → 5-{[(5-Chloropyridin-2-yl)methyl]sulfanyl}-3-(methoxymethoxy)-1-(methoxymethyl)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[CH:32]=[CH:31][C:30]([Cl:33])=[CH:29][N:28]=1>>[Cl:33][C:30]1[CH:31]=[CH:32][C:27]([CH2:26][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)=[N:28][CH:29]=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-5-chloropyridine instead of 1-(chloromethyl)-4-ethylbenzene.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-e7287ba653534dd3afc3bfb319fb587d
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09180122B2
Reaction notes
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