Hydrochloric Acid → 4-(3,5-Dichloro-phenyl)-6-[(6chloro-pyridin-3-yl)-hydroxy-(3-methyl-3h-imidazol4-yl)-methyl]-1h-quinolin-2-one

HRID 1384345Notes

Reaction equation

HRID 1384345 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2[C:18]3[C:13](=[CH:14][CH:15]=[C:16]([C:19]([C:27]4[CH:28]=[N:29][C:30]([Cl:33])=[CH:31][CH:32]=4)([C:21]4[N:22]([CH3:26])[CH:23]=[N:24][CH:25]=4)[OH:20])[CH:17]=3)[N:12]=[C:11]([O:34]C)[CH:10]=2)[CH:5]=[C:6]([Cl:8])[CH:7]=1.Cl>C1COCC1>[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2[C:18]3[C:13](=[CH:14][CH:15]=[C:16]([C:19]([C:27]4[CH:28]=[N:29][C:30]([Cl:33])=[CH:31][CH:32]=4)([OH:20])[C:21]4[N:22]([CH3:26])[CH:23]=[N:24][CH:25]=4)[CH:17]=3)[NH:12][C:11](=[O:34])[CH:10]=2)[CH:5]=[C:6]([Cl:8])[CH:7]=1

Participants

4

Procedure

Following the same procedure as described in example 1F, [4-(3,5-dichloro-phenyl)-2-methoxy-quinolin-6-yl]-(6-chloro-pyridin-3-yl)-(3-methyl-3H-imidazol-4-yl)-methanol (886 mg, 1.68 mmol) was treated with HCl in aqueous THF to yield the title compound of 16D. It was directly used for the next reaction without further purification.

Sources & evidence

ORD record
ord-dddc8a861e31490c9d3dde946a0780d6
Source dataset
uspto-grants-2001_07
Patent number
US06258824B1

Reaction notes

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