Reaction equation
[Cl:1][C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][C:3]=1[N:9]=[C:10]=[S:11].[Cl:12][C:13]1[CH:18]=[CH:17][C:16]([N:19]2[C:23]([C:24]#[N:25])=[CH:22][C:21]([CH3:26])=[N:20]2)=[CH:15][CH:14]=1>>[Cl:1][C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][C:3]=1[NH:9][C:10]([NH:25][CH2:24][C:23]1[N:19]([C:16]2[CH:17]=[CH:18][C:13]([Cl:12])=[CH:14][CH:15]=2)[N:20]=[C:21]([CH3:26])[CH:22]=1)=[S:11]Participants
3
Procedure
Prepared in 56% yield from 2,3-dichlorophenylisothiocyanate and the product of Example 205A according to the procedure described for Example 153B.
Sources & evidence
- ORD record
- ord-22c29d30724c4663a75cf358605e63eb
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07723367B2
Linked notes
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