Benzoyl isothiocyanate → HCID 86631506, compound
Reaction equation
[C:1]([N:9]=[C:10]=[S:11])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:12][C:13]1[C:18]([O:19][C:20]2[CH:27]=[CH:26][C:23]([C:24]#[N:25])=[CH:22][CH:21]=2)=[CH:17][C:16]([Br:28])=[CH:15][N:14]=1>>[C:1]([NH:9][C:10]([NH:12][C:13]1[C:18]([O:19][C:20]2[CH:21]=[CH:22][C:23]([C:24]#[N:25])=[CH:26][CH:27]=2)=[CH:17][C:16]([Br:28])=[CH:15][N:14]=1)=[S:11])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
Prepared according to the method of Example 7, step C from benzoyl isothiocyanate and 4-(2-amino-5-bromopyridin-3-yloxy)benzonitrile.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-56784d3847954a6eaf0cc683d364f814
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08883828B2
Reaction notes
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