Potassium Iodide → methyl (S)-2-(4-methanesulfonylpiperazin-1-yl)-3-[4-(2-methylquinolin-4-ylmethoxy)benzenesulfonylamino]propanoate

HRID 1966107Notes

Reaction equation

HRID 1966107 reaction equation
C(=O)([O-])[O-].[Cs+].[Cs+].Cl[CH2:8][C:9]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[N:12]=[C:11]([CH3:19])[CH:10]=1.[I-].[K+].[OH:22][C:23]1[CH:28]=[CH:27][C:26]([S:29]([NH:32][CH2:33][C@H:34]([N:39]2[CH2:44][CH2:43][N:42]([S:45]([CH3:48])(=[O:47])=[O:46])[CH2:41][CH2:40]2)[C:35]([O:37][CH3:38])=[O:36])(=[O:31])=[O:30])=[CH:25][CH:24]=1>CC(C)=O>[CH3:48][S:45]([N:42]1[CH2:41][CH2:40][N:39]([C@@H:34]([CH2:33][NH:32][S:29]([C:26]2[CH:25]=[CH:24][C:23]([O:22][CH2:8][C:9]3[C:18]4[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=4)[N:12]=[C:11]([CH3:19])[CH:10]=3)=[CH:28][CH:27]=2)(=[O:31])=[O:30])[C:35]([O:37][CH3:38])=[O:36])[CH2:44][CH2:43]1)(=[O:46])=[O:47]

Participants

6

Procedure

280 mg (0.85 mmol) of cesium carbonate followed by 160 mg (0.85 mmol) of 4-chloromethyl-2-methylquinoline and by 15 mg of potassium iodide are added to a solution of 300 mg (0.71 mmol) of methyl (S)-3-(4-hydroxybenzenesulfonylamino)-2-(4-methanesulfonylpiperazin-1-yl)propanoate in 10 ml of acetone. The reaction medium is stirred at ambient temperature for 18 h, filtered and concentrated under vacuum. The crude product is purified by chromatography on silica gel, elution being carried out with a 40/60 heptane/ethyl acetate mixture. 130 mg (32%) of methyl (S)-2-(4-methanesulfonylpiperazin-1-yl)-3-[4-(2-methylquinolin-4-ylmethoxy)benzenesulfonylamino]propanoate are obtained in the form of a white solid.

Workup

  1. filtrationfiltered
  2. concentrationconcentrated under vacuum
  3. customThe crude product is purified by chromatography on silica gel, elution

Sources & evidence

ORD record
ord-83fe38e4ed2748eab068ae5bb1b11724
Source dataset
uspto-grants-2013_04
Patent number
US08420632B2

Reaction notes

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