2-Bromo-6,7-dichloro-3-trifluoromethylquinoxaline → 2-Benzoxazol-2-yl-6,7-Dichloro-3-trifluoromethylquinoxaline

Reaction equation

Br[C:2]1[C:11]([C:12]([F:15])([F:14])[F:13])=[N:10][C:9]2[C:4](=[CH:5][C:6]([Cl:17])=[C:7]([Cl:16])[CH:8]=2)[N:3]=1.S[C:19]1[O:20][C:21]2[CH:27]=[CH:26][CH:25]=[CH:24][C:22]=2[N:23]=1>>[O:20]1[C:21]2[CH:27]=[CH:26][CH:25]=[CH:24][C:22]=2[N:23]=[C:19]1[C:2]1[C:11]([C:12]([F:15])([F:14])[F:13])=[N:10][C:9]2[C:4](=[CH:5][C:6]([Cl:17])=[C:7]([Cl:16])[CH:8]=2)[N:3]=1

Participants

Reactant 2

HCID 223411132-Bromo-6,7-dichloro-3-trifluoromethylquinoxaline

HCID 178418282CID 16943

Product 1

HCID 223412122-Benzoxazol-2-yl-6,7-Dichloro-3-trifluoromethylquinoxaline

Procedure

The title compound was prepared from 2-bromo-6,7-dichloro-3-trifluoromethylquinoxaline and 2-mercaptobenzoxazole in analogy with the method outlined in example 1.

Sources & evidence

ORD record: ord-90f3f976088c45569afecca675cffc2f
Source dataset: uspto-grants-2005_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06927214B1

Reaction notes

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