m-Chloroperbenzoic acid → HCID 18923325, compound

HRID 1900038Notes

Reaction equation

HRID 1900038 reaction equation
[Br:1][C:2]1[N:6]2[CH:7]=[CH:8][CH:9]=[C:10]([O:11][CH2:12][C:13]3[C:18]([Cl:19])=[CH:17][CH:16]=[C:15]([N:20]([CH3:34])[C:21](=[O:33])[CH2:22][NH:23][C:24](=[O:32])[CH2:25][N:26]4[CH2:31][CH2:30][S:29][CH2:28][CH2:27]4)[C:14]=3[Cl:35])[C:5]2=[N:4][C:3]=1[CH3:36].ClC1C=CC=C(C(OO)=[O:45])C=1>C(Cl)Cl>[Br:1][C:2]1[N:6]2[CH:7]=[CH:8][CH:9]=[C:10]([O:11][CH2:12][C:13]3[C:18]([Cl:19])=[CH:17][CH:16]=[C:15]([N:20]([CH3:34])[C:21](=[O:33])[CH2:22][NH:23][C:24](=[O:32])[CH2:25][N:26]4[CH2:27][CH2:28][S:29](=[O:45])[CH2:30][CH2:31]4)[C:14]=3[Cl:35])[C:5]2=[N:4][C:3]=1[CH3:36]

Participants

4

Procedure

To a solution of 3-bromo-8-[2,6-dichloro-3-[N-methyl-N-[(thiomorpholinoacetyl)glycyl]amino]benzyloxy]-2-methylimidazo[1,2-a]pyridine (200 mg) in methylene chloride (2 ml) was added m-chloroperbenzoic acid (80% purity, 76 mg) under ice-bath cooling, and the mixture was stirred for 1 hour at the same temperature. The reaction mixture was washed with water twice and brine, dried over magnesium sulfate, and concentrated in vacuo. The residue was purified by preparative thin layer chromatography (methylene chloride:methanol=5:1, V/V) to give 3-bromo-8-[2,6-dichloro-3-[N-methyl-N-[[(1-oxothiomorpholino)acetyl]glycyl]amino]benzyloxy]-2-methylimidazo[1,2-a]pyridine (96 mg ) as an amorphous.

Workup

  1. temperaturecooling
  2. washThe reaction mixture was washed with water twice
  3. dry with materialbrine, dried over magnesium sulfate
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by preparative thin layer chromatography (methylene chloride:methanol=5:1, V/V)

Sources & evidence

ORD record
ord-b6cd4b461c38467a9e53c6069f50205b
Source dataset
uspto-grants-1996_11
Patent number
US05574042

Reaction notes

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