Trifluoroacetic acid → HCID 86755345, compound
Reaction equation
C(OC([N:8]1[C:12]2[CH2:13][C@H:14]([C:30](=[O:48])[NH:31][CH2:32][CH2:33][C:34]3[N:35]([CH2:39][C:40]4[CH:45]=[CH:44][C:43]([C:46]#[N:47])=[CH:42][CH:41]=4)[CH:36]=[N:37][CH:38]=3)[CH:15](C(OC(C)(C)C)=O)[N:16]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[C:11]=2[N:10]=[CH:9]1)=O)(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[C:46]([C:43]1[CH:42]=[CH:41][C:40]([CH2:39][N:35]2[C:34]([CH2:33][CH2:32][NH:31][C:30]([C@H:14]3[CH2:13][C:12]4[NH:8][CH:9]=[N:10][C:11]=4[N:16]([C:17]4[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=4)[CH2:15]3)=[O:48])=[CH:38][N:37]=[CH:36]2)=[CH:45][CH:44]=1)#[N:47]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 6(S)-{2-[3-(4-cyano-benzyl)-3H-imidazol-4yl]ethylcarbamoyl}-4-phenyl-6,7-dihydro-4H-imidazo [4,5-]pyridine-1,5-dicarboxylic acid di-tert-butyl ester (0.58 g) in CH2Cl2 (10 ml) was added TFA (5 ml) and the solution was stirred 45 min. The solvents were removed in vacuo and the crude product was purified by preparative HPLC to obtain diastereomer A and diastereomer B as the title compounds.
Workup
- customThe solvents were removed in vacuo
- customthe crude product was purified by preparative HPLC
Sources & evidence
- ORD record
- ord-a5f201335910441786db901799b0c917
- Source dataset
- uspto-grants-2000_04
- Patent number
- US06054466
Reaction notes
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