Isocyanate → 3-(4,4'-dichlorobenzhydryloxy)-N-(cyclohexyl)azetidine-1-carboxamide
Reaction equation
Cl[C:2]1[CH:20]=CC(C(OC2CNC2)C2C=CC(Cl)=CC=2)=C[CH:3]=1.[N-]=C=O.Cl[C:25]1[CH:50]=[C:49]([Cl:51])[CH:48]=[CH:47][C:26]=1[CH:27]([O:35][CH:36]1[CH2:39][N:38]([C:40]([NH:42][C:43]([CH3:46])(C)[CH3:44])=[O:41])[CH2:37]1)[C:28]1[CH:33]=[CH:32][C:31]([Cl:34])=[CH:30][CH:29]=1>>[Cl:34][C:31]1[CH:30]=[CH:29][C:28]([CH:27]([O:35][CH:36]2[CH2:39][N:38]([C:40]([NH:42][CH:43]3[CH2:44][CH2:20][CH2:2][CH2:3][CH2:46]3)=[O:41])[CH2:37]2)[C:26]2[CH:47]=[CH:48][C:49]([Cl:51])=[CH:50][CH:25]=2)=[CH:33][CH:32]=1Participants
4
Procedure
This material was prepared from 3-(4,4′-dichlorobenzhydryloxy)azetidine (36) and the corresponding commercially available isocyanate, using the procedure described for compound (5).
Sources & evidence
- ORD record
- ord-9a5b7c4b2fa44f2eb5ea7d3add9360e7
- Source dataset
- uspto-grants-2009_03
- Patent number
- US07504522B2
Reaction notes
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