3,5-Dichlorophenyl isothiocyanate → HCID 54157895, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([F:17])=[C:6]([CH:16]=1)[C:7]([NH:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:8].[Cl:18][C:19]1[CH:20]=[C:21]([N:26]=[C:27]=[S:28])[CH:22]=[C:23]([Cl:25])[CH:24]=1>>[Cl:18][C:19]1[CH:20]=[C:21]([NH:26][C:27](=[S:28])[NH:1][C:2]2[CH:3]=[CH:4][C:5]([F:17])=[C:6]([CH:16]=2)[C:7]([NH:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[O:8])[CH:22]=[C:23]([Cl:25])[CH:24]=1Participants
3
Procedure
Prepared according to the procedure described for Example 60 using 5-amino-2-fluoro-N-phenyl-benzamide (0.920 g, 4.00 mmol) and 3,5-dichlorophenyl isothiocyanate (0.817 g, 4.00 mmol) to afford the product (1.52 g); m.p. 195-196° C.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-c5f2539b4d1b44be9a86e4c907d65635
- Source dataset
- uspto-grants-2001_07
- Patent number
- US06268387B1
Reaction notes
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