3,5-Dichloro-4-methylpyridine → HCID 66882488, compound

HRID 2242080Notes

Reaction equation

HRID 2242080 reaction equation
[Cl:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([Cl:9])[C:7]=1[CH3:8].[CH:10]1([CH2:13][O:14][C:15]2[CH:16]=[C:17]([CH:21]=[CH:22][C:23]=2[O:24][CH3:25])[C:18](Cl)=[O:19])[CH2:12][CH2:11]1>>[CH:10]1([CH2:13][O:14][C:15]2[CH:16]=[C:17](/[C:18](/[O:19][C:18](=[O:19])[C:17]3[CH:21]=[CH:22][C:23]([O:24][CH3:25])=[C:15]([O:14][CH2:13][CH:10]4[CH2:12][CH2:11]4)[CH:16]=3)=[CH:8]/[C:7]3[C:6]([Cl:9])=[CH:5][N:4]=[CH:3][C:2]=3[Cl:1])[CH:21]=[CH:22][C:23]=2[O:24][CH3:25])[CH2:12][CH2:11]1

Participants

3

Reactant 2

HCID 109538273,5-Dichloro-4-methylpyridineHCID 21187921HCID 21187921, compound

Product 1

HCID 66882488HCID 66882488, compound

Procedure

The compound was obtained starting from 3,5-dichloro-4-methyl-pyridine and 3-(cyclopropylmethoxy)-4-methoxy-benzoyl chloride, following the procedure of Example 31.

Workup

  1. customThe compound was obtained

Sources & evidence

ORD record
ord-e1039261418c40c69f1081e5991c41d9
Source dataset
uspto-grants-2010_03
Patent number
US07671066B2

Reaction notes

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