Benzyl Isothiocyanate → HCID 1327826, 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.[CH3:21][O:22][C:23]1[CH:30]=[CH:29][C:26]([CH2:27]Br)=[CH:25][CH:24]=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][CH2:27][C:26]1[CH:29]=[CH:30][C:23]([O:22][CH3:21])=[CH:24][CH:25]=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-methoxybenzyl bromide as the starting materials. (M+H)+−388.
Workup
- customThis compound was synthesized
Sources & evidence
- ORD record
- ord-f109436115764f3484be63251f425193
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07563905B2
Reaction notes
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