Benzyl isocyanate → HCID 86651112, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:30])[C@H:4]([C:6]1[CH:7]=[C:8]([C:16]2[CH:21]=[CH:20][C:19]([C:22]([F:25])([F:24])[F:23])=[CH:18][C:17]=2[CH2:26][NH:27][CH2:28][CH3:29])[CH:9]=[C:10]([C:12]([F:15])([F:14])[F:13])[CH:11]=1)[CH3:5].[CH2:31]([N:38]=[C:39]=[O:40])[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1>>[CH3:1][O:2][C:3](=[O:30])[C@H:4]([C:6]1[CH:7]=[C:8]([C:16]2[CH:21]=[CH:20][C:19]([C:22]([F:23])([F:24])[F:25])=[CH:18][C:17]=2[CH2:26][N:27]([CH2:28][CH3:29])[C:39]([NH:38][CH2:31][C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)=[O:40])[CH:9]=[C:10]([C:12]([F:14])([F:15])[F:13])[CH:11]=1)[CH3:5]Participants
3
Procedure
Prepared according to the procedure described in Example 43, Step 3, using the following starting materials: (S)-2-(2′-ethylaminomethyl-5,4′-bis-trifluoromethyl-biphenyl-3-yl)-propionic acid methyl ester and benzyl isocyanate.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-2182b40ecbcc4754b3691f3e6d1eb51b
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08362044B2
Reaction notes
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