3-Benzyloxy-4-methoxybenzoyl chloride → HCID 24825927, compound

HRID 2242066Notes

Reaction equation

HRID 2242066 reaction equation
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:15]=[CH:16][C:17]=1[O:18][CH3:19])[C:12](Cl)=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH:20]1([O:25][C:26]2[CH:27]=[C:28]([C:34](=[O:44])[CH2:35][C:36]3[C:41]([Cl:42])=[CH:40][N:39]=[CH:38][C:37]=3[Cl:43])[CH:29]=[CH:30][C:31]=2[O:32][CH3:33])[CH2:24][CH2:23][CH2:22][CH2:21]1>>[CH:20]1([O:25][C:26]2[CH:27]=[C:28](/[C:34](/[O:44][C:12](=[O:13])[C:11]3[CH:15]=[CH:16][C:17]([O:18][CH3:19])=[C:9]([O:8][CH2:1][C:2]4[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=4)[CH:10]=3)=[CH:35]/[C:36]3[C:41]([Cl:42])=[CH:40][N:39]=[CH:38][C:37]=3[Cl:43])[CH:29]=[CH:30][C:31]=2[O:32][CH3:33])[CH2:24][CH2:23][CH2:22][CH2:21]1

Participants

3

Procedure

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

Workup

  1. customThe compound was obtained

Sources & evidence

ORD record
ord-8020b2f99fc34d5fb9e0fa7f088fa3f5
Source dataset
uspto-grants-2010_03
Patent number
US07671066B2

Reaction notes

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