Isopropyl iodide → HCID 22479275, compound
Reaction equation
I[CH:2]([CH3:4])[CH3:3].[OH:5][C:6]1[CH:30]=[CH:29][C:9]([CH2:10][C:11]23[CH2:18][CH2:17][CH2:16][N:15]2[C:14](=[O:19])[N:13]([C:20]2[CH:25]=[C:24]([Cl:26])[N:23]=[C:22]([Cl:27])[CH:21]=2)[C:12]3=[O:28])=[CH:8][CH:7]=1>CN(C=O)C.C(O)(=O)CC(CC(O)=O)(C(O)=O)O>[CH:2]([O:5][C:6]1[CH:7]=[CH:8][C:9]([CH2:10][C:11]23[CH2:18][CH2:17][CH2:16][N:15]2[C:14](=[O:19])[N:13]([C:20]2[CH:21]=[C:22]([Cl:27])[N:23]=[C:24]([Cl:26])[CH:25]=2)[C:12]3=[O:28])=[CH:29][CH:30]=1)([CH3:4])[CH3:3]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
2-Iodopropane (0.5 ml) was added to a suspension of Example 196 (0.17 g) and CS2CO3 (0.28 g) in DMF (3 mL) and the mixture was stirred for 4 hours. The mixture was diluted with citric acid and the solution was extracted with EtOAc. EtOAc layer was washed with water and brine, dried and evaporated. The residue was purified via HPLC to yield the titled compound (0.13 g). MS m/z 435(MH+).
Workup
- extractionthe solution was extracted with EtOAc
- washEtOAc layer was washed with water and brine
- customdried
- customevaporated
- customThe residue was purified via HPLC
Sources & evidence
- ORD record
- ord-8d190ca2bf1d47f3bcd492229fad4d9a
- Source dataset
- uspto-grants-2008_03
- Patent number
- US07342012B2
Reaction notes
Loading…