Benzyl isocyanate → HCID 18663214, compound
Reaction equation
[F:1][C:2]1[CH:30]=[CH:29][C:5]2[C:6]([CH:9]3[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][N:17]4[CH2:21][CH2:20][N:19](C5C=CC=CC=5)[C:18]4=[O:28])[CH2:11][CH2:10]3)=[N:7][O:8][C:4]=2[CH:3]=1.[CH2:31](N=C=O)[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1>>[CH2:31]([N:19]1[CH2:20][CH2:21][N:17]([CH2:16][CH2:15][N:12]2[CH2:13][CH2:14][CH:9]([C:6]3[C:5]4[CH:29]=[CH:30][C:2]([F:1])=[CH:3][C:4]=4[O:8][N:7]=3)[CH2:10][CH2:11]2)[C:18]1=[O:28])[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1Participants
3
Procedure
This product is obtained in the same manner as the compound of Example 5, but with replacement of the phenyl isocyanate by benzyl isocyanate in Step 1 of the synthesis. The expected product melts at 126°-130° C.
Sources & evidence
- ORD record
- ord-b8783605f4644c4991b91bfb4b9b0fa3
- Source dataset
- uspto-grants-1998_07
- Patent number
- US05780474
Reaction notes
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