Veratroyl chloride → HCID 24825929, compound

HRID 2242075Notes

Reaction equation

HRID 2242075 reaction equation
[CH:1]1([O:6][C:7]2[CH:8]=[C:9]([CH:13]=[CH:14][C:15]=2[O:16][CH3:17])[C:10](Cl)=[O:11])[CH2:5][CH2:4][CH2:3][CH2:2]1.[Cl:18][C:19]1[CH:20]=[N:21][CH:22]=[C:23]([Cl:26])[C:24]=1[CH3:25].[CH3:27][O:28][C:29]1[CH:30]=[C:31]([CH:35]=[CH:36][C:37]=1[O:38][CH3:39])[C:32](Cl)=[O:33]>>[CH3:27][O:28][C:29]1[CH:30]=[C:31]([CH:35]=[CH:36][C:37]=1[O:38][CH3:39])[C:32]([O:11]/[C:10](/[C:9]1[CH:13]=[CH:14][C:15]([O:16][CH3:17])=[C:7]([O:6][CH:1]2[CH2:5][CH2:4][CH2:3][CH2:2]2)[CH:8]=1)=[CH:25]\[C:24]1[C:23]([Cl:26])=[CH:22][N:21]=[CH:20][C:19]=1[Cl:18])=[O:33]

Participants

4

Reactant 3

HCID 77070Veratroyl chlorideHCID 27946003-(Cyclopentyloxy)-4-methoxybenzoyl chlorideHCID 109538273,5-Dichloro-4-methylpyridine

Product 1

HCID 24825929HCID 24825929, compound

Procedure

The compound was obtained starting from 3-cyclopentyloxy-4-methoxy-benzoyl chloride, 3,5-dichloro-4-methylpyridine and 3,4-dimethoxy-benzoyl chloride, following the procedure of Example 24.

Workup

  1. customThe compound was obtained

Sources & evidence

ORD record
ord-9d2d42b8477344b7b03fe5e2f01bd315
Source dataset
uspto-grants-2010_03
Patent number
US07671066B2

Reaction notes

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