Potassium Carbonate → 4-(Quinolin-2-yl-methoxy)phenyl cycloheptyl ketone

HRID 484348Notes

Reaction equation

HRID 484348 reaction equation
[CH:1]1([C:8]([C:10]2[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][CH:11]=2)=[O:9])[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.Cl.Cl[CH2:19][C:20]1[CH:29]=[CH:28][C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[N:21]=1.C(=O)([O-])[O-].[K+].[K+]>>[CH:1]1([C:8]([C:10]2[CH:15]=[CH:14][C:13]([O:16][CH2:19][C:20]3[CH:29]=[CH:28][C:27]4[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=4)[N:21]=3)=[CH:12][CH:11]=2)=[O:9])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7]1

Participants

4

Reactant 3

HCID 11430Potassium CarbonateHCID 30838232-(Chloromethyl)quinoline hydrochlorideHCID 200842354-Hydroxyphenyl cycloheptyl ketone

Product 1

HCID 200842384-(Quinolin-2-yl-methoxy)phenyl cycloheptyl ketone

Procedure

In analogy to the procedure of Example III, the title compound is prepared from 10 g (45.8 mmol) of the compound from Example XII, 10.3 g (48.1 mmol) of 2-chloromethylquinoline hydrochloride and 13.8 g (0.10 mol) of potassium carbonate.

Sources & evidence

ORD record
ord-f451e15b71ce4aa391b4790ae11ceead
Source dataset
uspto-grants-1993_07
Patent number
US05231103

Reaction notes

Loading…