3-Amino-5-methylisoxazole → HCID 14368606, compound

HRID 1089460Notes

Reaction equation

HRID 1089460 reaction equation
[NH2:1][C:2]1[CH:6]=[C:5]([CH3:7])[O:4][N:3]=1.[OH:8][C:9]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[N:12]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:11][C:10]=1[C:25](OCC)=[O:26]>C1(C)C=CC=CC=1.[O-2].[O-2].[Mn+4]>[CH3:7][C:5]1[O:4][N:3]=[C:2]([NH:1][C:25]([C:10]2[C:9](=[O:8])[C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[N:12]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH:11]=2)=[O:26])[CH:6]=1

Participants

5

Reactant 2

HCID 661723-Amino-5-methylisoxazoleHCID 85585358HCID 85585358, compound

Product 1

HCID 14368606HCID 14368606, compoundYield 49.6%

Reagents, catalysts & solvents 2

HCID 178418406HCID 178418406, compoundCatalystHCID 1140TolueneSolvent

Procedure

A solution of 6.0 g of 3-amino-5-methylisoxazole and 10 g of 1,2-dihydro-4-hydroxy-1-phenyl-3-quinolinecarboxylic acid, ethyl ester in 150 ml of toluene was refluxed for 16 hours in a soxhlet apparatus containing 10 g of 4 Å molecular sieves. The solution was cooled to room temperature, treated with 30 g of activated manganese dioxide, stirred for three hours at 30° C., and filtered. Evaporation of the volatiles afforded a residue which was purified by means of high pressure liquid chromatography (silica gel: 1% methanol-dichloromethane as the eluent) to yield 5.8 g (49%) of 1,4-dihydro-N-(5-methyl-3-isoxazolyl)-4-oxo-1-phenyl-3-quinolinecarboxamide m.p. 163°-164° C.

Workup

  1. additioncontaining 10 g of 4 Å molecular sieves
  2. filtrationfiltered
  3. customEvaporation of the volatiles
  4. customafforded a residue which
  5. customwas purified by means of high pressure liquid chromatography (silica gel

Sources & evidence

ORD record
ord-f7628f5d4157452bbe4f2aec7f0eb472
Source dataset
uspto-grants-1990_10
Patent number
US04966906

Reaction notes

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