Hydrochloric Acid → 5-(3-(4-bromophenyl)-3-(4-methylthiazol-5-yl)propanoyl)pyridin-2(1H)-one

HRID 1617902Notes

Reaction equation

HRID 1617902 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:20]2[S:24][CH:23]=[N:22][C:21]=2[CH3:25])[CH2:9][C:10]([C:12]2[CH:13]=[N:14][C:15]([O:18]C)=[CH:16][CH:17]=2)=[O:11])=[CH:4][CH:3]=1.Cl>O1CCOCC1>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:20]2[S:24][CH:23]=[N:22][C:21]=2[CH3:25])[CH2:9][C:10]([C:12]2[CH:17]=[CH:16][C:15](=[O:18])[NH:14][CH:13]=2)=[O:11])=[CH:4][CH:3]=1

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 666668163-(4-Bromophenyl)-1-(6-methoxypyridin-3-yl)-3-(4-methylthiazol-5-yl)propan-1-one

Product 1

HCID 666685555-(3-(4-bromophenyl)-3-(4-methylthiazol-5-yl)propanoyl)pyridin-2(1H)-one

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

In analogy to example 162, step 2, 3-(4-bromophenyl)-1-(6-methoxypyridin-3-yl)-3-(4-methylthiazol-5-yl)propan-1-one was reacted with concentrated aqueous HCl in 1,4-dioxane to give the title compound as an yellow solid, MS (ESI+): m/z=405.2 [M+H]+.

Sources & evidence

ORD record
ord-0b6384698c654928ad7bf29ab98e33f8
Source dataset
uspto-grants-2014_07
Patent number
US08765730B2

Reaction notes

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