Phenyl isocyanate → HCID 10128505, compound
Reaction equation
[C:1]1([N:7]=[C:8]=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(NC([N:17]1[CH2:22][CH2:21][CH:20]([N:23]2[N:32]=[C:31]([C:33]3[CH:38]=[CH:37][C:36]([O:39][CH2:40][CH3:41])=[C:35]([O:42][CH2:43][CH3:44])[CH:34]=3)[C@@H:30]3[C@@H:25]([CH2:26][CH:27]=[CH:28][CH2:29]3)[C:24]2=[O:45])[CH2:19][CH2:18]1)=O)(C)(C)C>>[C:1]1([NH:7][C:8]([N:17]2[CH2:22][CH2:21][CH:20]([N:23]3[N:32]=[C:31]([C:33]4[CH:38]=[CH:37][C:36]([O:39][CH2:40][CH3:41])=[C:35]([O:42][CH2:43][CH3:44])[CH:34]=4)[C@@H:30]4[C@@H:25]([CH2:26][CH:27]=[CH:28][CH2:29]4)[C:24]3=[O:45])[CH2:19][CH2:18]2)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
3
Procedure
Prepared from starting compound A2 and phenylisocyanate as described for compound 6. Crystallisation from ether. M.p. 109-112° C.
Workup
- customPrepared
- customCrystallisation from ether
Sources & evidence
- ORD record
- ord-97761a1937644ca19f1baa980a6ed9fb
- Source dataset
- uspto-grants-2009_05
- Patent number
- US07531540B2
Reaction notes
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