HCID 59516907, compound → HCID 59517045, compound

HRID 1698618Notes

Reaction equation

HRID 1698618 reaction equation
[CH3:1][S:2][C:3](=[NH:25])[CH:4]([NH:16][C:17]1[CH:22]=[CH:21][C:20]([C:23]#[N:24])=[CH:19][CH:18]=1)[C:5]1[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[C:7]([O:13][CH3:14])[C:6]=1[F:15]>C(OCC)(=O)C.[O-2].[O-2].[Mn+4]>[CH3:1][S:2][C:3](=[NH:25])[C:4](=[N:16][C:17]1[CH:18]=[CH:19][C:20]([C:23]#[N:24])=[CH:21][CH:22]=1)[C:5]1[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[C:7]([O:13][CH3:14])[C:6]=1[F:15]

Participants

4

Reactant 1

HCID 59516907HCID 59516907, compound

Product 1

HCID 59517045HCID 59517045, compoundYield 98.6%

Reagents, catalysts & solvents 2

HCID 178418406HCID 178418406, compoundCatalystHCID 8857Ethyl AcetateSolvent

Procedure

After adding 4.95 g of manganese dioxide to a solution of 2.05 g of 2-(4-cyanophenylamino)-2-(2-fluoro-3,5-dimethoxyphenyl)thioacetimidic acid methyl ester in 100 ml of ethyl acetate, the mixture was stirred at room temperature for 3 hours. The reaction mixture was filtered through celite, and the celite was washed with 500 ml of ethyl acetate. The organic layers were combined and concentrated under reduced pressure. The title compound (2.01 g) was obtained as a light yellow solid.

Workup

  1. filtrationThe reaction mixture was filtered through celite
  2. washthe celite was washed with 500 ml of ethyl acetate
  3. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-5ab37f80e4cd4b6aad1415f32f8efad4
Source dataset
uspto-grants-2012_04
Patent number
US08163787B2

Reaction notes

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