2-Aminophenol → (2R,4S)-4-(Aminomethyl)-N-[(5-phenyloxy-2-benzimidazolyl)methyl]-2-pyrrolidinecarboxamide
Reaction equation
C(OC([NH:11][CH2:12][C:13](O)=O)=O)C1C=CC=CC=1.NC1C=CC=CC=1O.[NH2:24][C:25]1[CH:30]=[CH:29][C:28]([O:31][C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)=[CH:27][C:26]=1[NH2:38].C(OC(NCC(N[C@H]1CN(C(OC(C)(C)C)=O)[C@H](C(O)=O)C1)=O)=O)(C)(C)C.C(OC([NH:73][CH2:74][C@@H:75]1[CH2:79][N:78](C(OC(C)(C)C)=O)[C@@H:77]([C:87]([OH:89])=O)[CH2:76]1)=O)(C)(C)C>>[NH2:73][CH2:74][C@H:75]1[CH2:79][NH:78][C@@H:77]([C:87]([NH:11][CH2:12][C:13]2[NH:38][C:26]3[CH:27]=[C:28]([O:31][C:32]4[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=4)[CH:29]=[CH:30][C:25]=3[N:24]=2)=[O:89])[CH2:76]1Participants
6
Reactant 5
Product 1
Procedure
This compound was prepared as in Compound M77, replacing N-(Benzyloxycarbonyl)-D-homophenylalanine with N-(Benzyloxycarbonyl)glycine, 2-aminophenol with 1,2-diamino-4-phenyloxybenzene and trans-4-(N-tert-butoxycarbonylglycyl)amino-N-tert-butoxycarbonyl-L-proline with trans-4-(N-tert-butoxycarbonylaminomethyl)-N-tert-butoxycarbonyl-D-proline.
Sources & evidence
- ORD record
- ord-3b8451be9e6949f7a156f5bbe319100b
- Source dataset
- uspto-grants-2002_06
- Patent number
- US06399629B1
Reaction notes
Loading…