Potassium Iodide → HCID 145823946, compound

HRID 2395875Notes

Reaction equation

HRID 2395875 reaction equation
[CH2:1]([O:4][C:5]([NH:7][C:8]([C:10]1[CH:15]=[CH:14][C:13]([N:16]2[CH2:20][C:19]([O:21][CH3:22])=[C:18]([C:23]3[CH:28]=[CH:27][C:26]([CH2:29][CH2:30][C:31]([OH:33])=[O:32])=[CH:25][CH:24]=3)[C:17]2=[O:34])=[CH:12][CH:11]=1)=[NH:9])=[O:6])[CH:2]=[CH2:3].[C:35]([O:41][CH2:42]Cl)(=[O:40])[C:36]([CH3:39])([CH3:38])[CH3:37].[I-].[K+].C(=O)([O-])O.[K+].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[CH2:1]([O:4][C:5]([NH:7][C:8]([C:10]1[CH:11]=[CH:12][C:13]([N:16]2[CH2:20][C:19]([O:21][CH3:22])=[C:18]([C:23]3[CH:24]=[CH:25][C:26]([CH2:29][CH2:30][C:31]([O:33][CH2:42][O:41][C:35](=[O:40])[C:36]([CH3:39])([CH3:38])[CH3:37])=[O:32])=[CH:27][CH:28]=3)[C:17]2=[O:34])=[CH:14][CH:15]=1)=[NH:9])=[O:6])[CH:2]=[CH2:3]

Participants

7

Reactant 5

HCID 4875Potassium IodideHCID 11430Potassium CarbonateHCID 87885Chloromethyl pivalateHCID 516893Potassium BicarbonateHCID 139627756HCID 139627756, compound

Product 1

HCID 145823946HCID 145823946, compound

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

Prepared by stirring a suspension of 1-[4-(allyloxycarbonyl-amidino)-phenyl]-3-[4-(2-carboxy-ethyl)-phenyl]-4-methoxy-3-pyrrolin-2-one, 2 equivalents of chloromethyl pivalate, 2 equivalents of potassium iodide, 2 equivalents of potassium hydrogen carbonate and 2 equivalents of potassium carbonate in dimethylformamide at ambient temperature for three days.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-fc4e4877929a42d5bf8a768d9d8c9e40
Source dataset
uspto-grants-1996_02
Patent number
US05489693

Reaction notes

Loading…