Benzyl isocyanate → HCID 66607711, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:26])[CH2:4][C:5]1[CH:6]=[C:7]([C:12]2[CH:17]=[CH:16][C:15]([C:18]([F:21])([F:20])[F:19])=[CH:14][C:13]=2[CH2:22][NH:23][CH2:24][CH3:25])[CH:8]=[C:9]([F:11])[CH:10]=1.[CH2:27]([N:34]=[C:35]=[O:36])[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>>[CH3:1][O:2][C:3](=[O:26])[CH2:4][C:5]1[CH:6]=[C:7]([C:12]2[CH:17]=[CH:16][C:15]([C:18]([F:19])([F:20])[F:21])=[CH:14][C:13]=2[CH2:22][N:23]([CH2:24][CH3:25])[C:35]([NH:34][CH2:27][C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)=[O:36])[CH:8]=[C:9]([F:11])[CH:10]=1Participants
3
Procedure
Prepared according to the procedure described in Example 95, Step 1, using the following starting materials: (2′-ethylaminomethyl-5-fluoro-4′-trifluoromethyl-biphenyl-3-yl)-acetic acid methyl ester and benzyl isocyanate.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-04f1cdf2c949459eb29f175e7983b980
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08362044B2
Reaction notes
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