Benzyl Isothiocyanate → HCID 11372757, compound
Reaction equation
[C:1]([NH:9][NH2:10])(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:11]([N:18]=[C:19]=[S:20])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[Cl:21][C:22]1[CH:29]=[CH:28][C:25]([CH2:26]Br)=[CH:24][CH:23]=1>>[CH2:11]([N:18]1[C:1]([C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[N:9][N:10]=[C:19]1[S:20][CH2:26][C:25]1[CH:28]=[CH:29][C:22]([Cl:21])=[CH:23][CH:24]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1Participants
4
Procedure
This compound was synthesized using the same methodology as described in Example 1 above, using benzoic acid hydrazide, benzyl isothiocyanate and 4-chlorobenzyl bromide as the starting materials.
Workup
- customThis compound was synthesized
Sources & evidence
- ORD record
- ord-80c21bbd57c14ac7b290c2e9cca2307b
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07563905B2
Reaction notes
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