Chloromethyl methyl sulfide → HCID 23442452, compound

HRID 2119658Notes

Reaction equation

HRID 2119658 reaction equation
[H-].[Na+].[CH2:3]([N:5]1[C:14]2[CH:13]=[CH:12][C:11]([CH3:15])=[CH:10][C:9]=2[C:8](=[O:16])[C:7]2[N:17]([CH3:20])[N:18]=[CH:19][C:6]1=2)[CH3:4].[CH3:21][S:22]CCl>CN(C)C=O.[Cl-].[Na+].O>[CH3:20][N:17]1[C:7]2[C:8](=[O:16])[C:9]3[CH:10]=[C:11]([CH3:15])[CH:12]=[CH:13][C:14]=3[N:5]([CH2:3][CH2:4][S:22][CH3:21])[C:6]=2[CH:19]=[N:18]1

Participants

6

Reactant 3

HCID 16916Chloromethyl methyl sulfide2×HCID 24758Sodium hydride2×HCID 23442433HCID 23442433, compound

Product 1

HCID 23442452HCID 23442452, compoundYield 43%

Reagents, catalysts & solvents 2

HCID 6228DimethylformamideSolventHCID 57417360Sodium chloride; waterSolvent

Conditions

Temperature
0 °C

Procedure

To a suspension of sodium hydride (60-72% in mineral oil, 225 mg, 5.6 mmol), which was washed with hexane and dried in vacuo, in N,N-dimethylformamide (40 ml) was added a solution of 1,7-dimethyl-1,4-dihydro-9H-pyrazolo[4,3-b]quinolin-9-one (EXAMPLE 47, step 2, 0.80 g, 3.75 mmol) in N,N-dimethylformamide at 0° C. The mixture was stirred at 0° C. for 10 min and at room temperature for 2 h. Chloromethyl methyl sulfide (0.87 ml, 7.5 mmol) was added at 0° C. and the mixture was stirred at room temperature for 10.5 h. Further more, sodium hydride (60-72% in mineral oil, 68 mg, 2.8 mmol) and chloromethyl methyl sulfide (0.87 ml, 7.5 mmol) were added. After 2 h, the mixture was heated at 50° C. for 15.5 h. The mixture was poured into brine (50 ml) and extracted with ethyl acetate (50 ml×2). The organic extracts were dried over magnesium sulfate and concentrated. Purification by column chromatography on silica gel eluting with ethyl acetate/hexane (1:1) gave 0.46 g (43%) of the title compound as a pale yellow solid.

Workup

  1. washwas washed with hexane
  2. dry with materialdried in vacuo, in N,N-dimethylformamide (40 ml)
  3. stirringthe mixture was stirred at room temperature for 10.5 h
  4. waitAfter 2 h
  5. temperaturethe mixture was heated at 50° C. for 15.5 h
  6. extractionextracted with ethyl acetate (50 ml×2)
  7. dry with materialThe organic extracts were dried over magnesium sulfate
  8. concentrationconcentrated
  9. customPurification by column chromatography on silica gel eluting with ethyl acetate/hexane (1:1)

Sources & evidence

ORD record
ord-8ef0e530b2ca40878922b6446dee655a
Source dataset
uspto-grants-2004_02
Patent number
US06686373B2

Reaction notes

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