Isopropyl iodide → HCID 22479275, compound

HRID 1392195Notes

Reaction equation

HRID 1392195 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

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

  1. extractionthe solution was extracted with EtOAc
  2. washEtOAc layer was washed with water and brine
  3. customdried
  4. customevaporated
  5. customThe residue was purified via HPLC

Sources & evidence

ORD record
ord-8d190ca2bf1d47f3bcd492229fad4d9a
Source dataset
uspto-grants-2008_03
Patent number
US07342012B2

Reaction notes

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