1,2-Dichloroethane → 1-(4-Cyanobenzyl)imidazole-5-acetic acid
Reaction equation
[Li+].[Cl-].Cl.C([O:7][C:8](=[O:24])[C@H:9](CCSC)NC(=O)[C@@H]1[C@@H](CC)CCN1)(C)C.[CH:25]1[CH:30]=[C:29]2[C:31]([N:33](O)N=N[C:28]2=[CH:27][CH:26]=1)=O.C(Cl)CCl.C[N:42]1[CH2:47]CO[CH2:44][CH2:43]1.[CH3:48][N:49](C=O)C>>[C:48]([C:26]1[CH:27]=[CH:28][C:29]([CH2:31][N:33]2[C:44]([CH2:9][C:8]([OH:24])=[O:7])=[CH:43][N:42]=[CH:47]2)=[CH:30][CH:25]=1)#[N:49]Participants
Procedure
LiCl (0.416 g, 1.47 mmol), pyrrolidin-2(S)-ylmethyl]-3(S)-ethyl-prolyl-methionine isopropyl ester hydrochloride (Step I) (0.63 g, 1.33 mmol), HOOBT (0.239 g, 1.47 mmol), and EDC (0.281 g, 1.47 mmol) were dissolved in degassed DMF (20 mL) with stirring at room temperature, N-methylmorpholine (0.8 mL, 5.32 mmol) was added to achieve a pH of 7, and stirring was continued overnight. The reaction mixture was concentrated to remove most of the DMF, and the residue was partitioned between EtOAc and aq satd NaHCO3 solution. The aq layer was washed with EtOAc, the organics combined, washed with brine and dried (MgSO4). Filtration and concentration to dryness gave the title compound after chromatography on silica gel eluting with CH2Cl2 :CH3OH, 95:5.
Workup
- stirringstirring
- concentrationThe reaction mixture was concentrated
- customto remove most of the DMF
- customthe residue was partitioned between EtOAc
- washThe aq layer was washed with EtOAc
- washwashed with brine
- dry with materialdried (MgSO4)
- filtrationFiltration and concentration to dryness
Sources & evidence
- ORD record
- ord-3b4676f16ee14592a1f33649ee5ade90
- Source dataset
- uspto-grants-1997_05
- Patent number
- US05627202
Reaction notes
Loading…