Thionyl Chloride → HCID 23444948, compound
Reaction equation
[ClH:1].[CH3:2][C:3]1[CH:4]=[C:5]([C:10]2[CH:11]=[C:12]([CH2:17]O)[C:13]([CH3:16])=[N:14][CH:15]=2)[CH:6]=[CH:7][C:8]=1[CH3:9].S(Cl)([Cl:21])=O>>[ClH:21].[Cl:1][CH2:17][C:12]1[C:13]([CH3:16])=[N:14][CH:15]=[C:10]([C:5]2[CH:6]=[CH:7][C:8]([CH3:9])=[C:3]([CH3:2])[CH:4]=2)[CH:11]=1Participants
3
Procedure
The title compound, MS: m/e=245.1 (M+) was obtained as a yellow solid (98% yield) by the reaction of [5-(3,4-dimethyl-phenyl)-2-methyl-pyridin-3-yl]-methanol hydrochloride (1:1) with thionyl chloride at 20° C. for 1 h then 2 h at reflux.
Sources & evidence
- ORD record
- ord-25b5e61e736f41f18986b6b75fc45f77
- Source dataset
- uspto-grants-2004_01
- Patent number
- US06683097B2
Reaction notes
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