Hydrochloric Acid → HCID 67015599, compound

HRID 1617652Notes

Reaction equation

HRID 1617652 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH2:20][CH2:21][CH2:22][C:23]([F:26])([F:25])[F:24])[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]([CH2:20][CH2:21][CH2:22][C:23]([F:26])([F:24])[F: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 67015533HCID 67015533, compound

Product 1

HCID 67015599HCID 67015599, compound

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

In analogy to example 162, step 2, 3-(4-bromo-phenyl)-7,7,7-trifluoro-1-(6-methoxy-pyridin-3-yl)-heptan-1-one was reacted with concentrated aqueous HCl in 1,4-dioxane to give the title compound as a light yellow oil, MS (ESI+): m/z=416.1 [M+H]+.

Sources & evidence

ORD record
ord-09fbdbf2993849138935ea4fd3ff6a5d
Source dataset
uspto-grants-2014_07
Patent number
US08765730B2

Reaction notes

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