Potassium Iodide → HCID 66590888, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH2:8][CH2:9][N:10]([CH2:16][C:17]2[O:18][CH:19]=[CH:20][CH:21]=2)[CH2:11][C:12]([NH:14][CH3:15])=[O:13])[CH:5]=[CH:6][CH:7]=1.[Cl:22][CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=1[F:30].C([O-])([O-])=O.[K+].[K+].[I-].[K+]>CN(C)C=O>[ClH:22].[F:30][C:25]1[CH:26]=[CH:27][CH:28]=[CH:29][C:24]=1[CH2:23][O:1][C:2]1[CH:3]=[C:4]([CH2:8][CH2:9][N:10]([CH2:16][C:17]2[O:18][CH:19]=[CH:20][CH:21]=2)[CH2:11][C:12]([NH:14][CH3:15])=[O:13])[CH:5]=[CH:6][CH:7]=1Participants
6
Procedure
A solution of 60 mg (0.21 mmol) of 2-[[2-(3-hydroxy-phenyl)-ethyl]-(furan-2-ylmethyl)-amino]-N-methyl-acetamide, 36 mg (0.25 mmol) of 1-chloromethyl-2-fluoro-benzene, 44 mg of K2CO3 (0.32 mmol) and 3 mg of potassium iodide in 4 ml of dimethylformamide was refluxed overnight. The solvent was removed under vacuum and the crude product was purified by preparative HPLC. The isolated product was dissolved in ethyl acetate/hydrochloric acid. The solvent was removed under vacuum and the residue was triturated with diethyl ether. 65 mg (72% yield) of the title compound were isolated as a white solid.
Workup
- customThe solvent was removed under vacuum
- customthe crude product was purified by preparative HPLC
- dissolutionThe isolated product was dissolved in ethyl acetate/hydrochloric acid
- customThe solvent was removed under vacuum
- customthe residue was triturated with diethyl ether
Sources & evidence
- ORD record
- ord-6e6617c037654263803febf894829b60
- Source dataset
- uspto-grants-2013_06
- Patent number
- US08470877B2
Reaction notes
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