Veratroyl chloride → HCID 66882805, compound

HRID 2242063Notes

Reaction equation

[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][C:11]=1[O:12][CH3:13])[C:6](Cl)=[O:7].[CH:14]1([CH2:17][O:18][C:19]2[CH:20]=[C:21]([C:27](=[O:37])[CH2:28][C:29]3[C:34]([Cl:35])=[CH:33][N:32]=[CH:31][C:30]=3[Cl:36])[CH:22]=[CH:23][C:24]=2[O:25][CH3:26])[CH2:16][CH2:15]1>>[CH:14]1([CH2:17][O:18][C:19]2[CH:20]=[C:21](/[C:27](/[O:37][C:6](=[O:7])[C:5]3[CH:9]=[CH:10][C:11]([O:12][CH3:13])=[C:3]([O:2][CH3:1])[CH:4]=3)=[CH:28]/[C:29]3[C:30]([Cl:36])=[CH:31][N:32]=[CH:33][C:34]=3[Cl:35])[CH:22]=[CH:23][C:24]=2[O:25][CH3:26])[CH2:16][CH2:15]1

Participants

Reactant 2

HCID 77070Veratroyl chloride

HCID 66881692HCID 66881692, compound

Product 1

HCID 66882805HCID 66882805, compound

Procedure

The compound was obtained starting from 3,4-dimethoxy-benzoyl chloride and 1-(3-cyclopropylmethoxy-4-methoxy-phenyl)-2-(3,5-dichloro -pyridin-4-yl)-ethanone, following the procedure of Example 7.

Workup

customThe compound was obtained

Sources & evidence

ORD record: ord-1d4d6c012416449c9725681c44c22aef
Source dataset: uspto-grants-2010_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07671066B2

Reaction notes

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