3-(Chloromethyl)pyridine → HCID 86731537, compound
Reaction equation
C([C:3]1C=[CH:23][C:6]([CH2:7][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)=[CH:5][CH:4]=1)C.ClCC1C=[N:29]C=CC=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][CH2:7][C:6]2[CH:23]=[N:29][CH:3]=[CH:4][CH:5]=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 3-chloromethylpyridine instead of 1-(chloromethyl)-4-ethylbenzene.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-85627c93bf074d44baf47710d6e2826f
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09180122B2
Reaction notes
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