2,6-Difluorobenzoyl isocyanate → HCID 13711427, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:10]([F:13])([F:12])[F:11])[C:5]([F:9])=[C:6]([CH:8]=1)[NH2:7].[F:14][C:15]1[CH:25]=[CH:24][CH:23]=[C:22]([F:26])[C:16]=1[C:17]([N:19]=[C:20]=[O:21])=[O:18]>>[Cl:1][C:2]1[CH:3]=[C:4]([C:10]([F:13])([F:11])[F:12])[C:5]([F:9])=[C:6]([NH:7][C:20]([NH:19][C:17](=[O:18])[C:16]2[C:22]([F:26])=[CH:23][CH:24]=[CH:25][C:15]=2[F:14])=[O:21])[CH:8]=1Participants
3
Procedure
The product was prepared from 5-chloro-2-fluoro-3-trifluoromethylaniline (0.5 g) and 2,6-difluorobenzoylisocyanate (0.4 g) by operating according to the process of Example 1 to obtain the product 0.6 g. (m.p. 187°-189° C.)
Sources & evidence
- ORD record
- ord-00c6126d9031443cb52cb2673fd31e84
- Source dataset
- uspto-grants-1987_12
- Patent number
- US04713396
Reaction notes
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