N-bromobutanimide → HCID 67383752, compound

HRID 245216Notes

Reaction equation

[CH2:1]([O:3][C:4]1[CH:13]=[C:12]2[C:7]([C:8]([C:25]([O:27][CH3:28])=[O:26])=[C:9]([CH3:24])[C:10]([C:14]3[CH:19]=[CH:18][CH:17]=[C:16]([C:20]([F:23])([F:22])[F:21])[CH:15]=3)=[N:11]2)=[CH:6][C:5]=1[S:29]([CH2:32][CH3:33])(=[O:31])=[O:30])[CH3:2].[Br:34]N1C(=O)CCC1=O>C(Cl)(Cl)(Cl)Cl>[Br:34][CH2:24][C:9]1[C:10]([C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([C:20]([F:23])([F:21])[F:22])[CH:15]=2)=[N:11][C:12]2[C:7]([C:8]=1[C:25]([O:27][CH3:28])=[O:26])=[CH:6][C:5]([S:29]([CH2:32][CH3:33])(=[O:31])=[O:30])=[C:4]([O:3][CH2:1][CH3:2])[CH:13]=2

Participants

Conditions

Temperature: 100 °C

Procedure

A mixture of methyl 7-(ethyloxy)-6-(ethylsulfonyl)-3-methyl-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate (9.11 g, 18.92 mmol), N-bromosuccinimide (4.38 g, 24.60 mmol) and diphenylperoxyanhydride (0.458 g, 1.892 mmol) in carbon tetrachloride (100 mL) was heated to 100° C. overnight. The mixture was cooled to room temperature and the solvent was removed under reduced pressure to afford methyl 3-(bromomethyl)-7-(ethyloxy)-6-(ethylsulfonyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate. This material was used without further purification. MS (m/z) 562.0 (M+H+).

Workup

temperatureThe mixture was cooled to room temperature
customthe solvent was removed under reduced pressure

Sources & evidence

ORD record: ord-ebe05362c3734ed3a19040451a956f39
Source dataset: uspto-grants-2014_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08658636B2

Reaction notes

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