Dimethylformamide → HCID 15868592, compound

HRID 2287292Notes

Reaction equation

HRID 2287292 reaction equation
CN(C)[CH:3]=[O:4].[CH2:6]([N:8]1[C:21]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[S:15][C:14]2[C:9]1=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH3:7].P(Cl)(Cl)(Cl)=O.[C:27](=O)([O-])[O-:28].[Na+].[Na+]>[Cl-].[Zn+2].[Cl-].O.C1(C)C=CC=CC=1>[CH:27]([C:12]1[CH:11]=[CH:10][C:9]2[N:8]([CH2:6][CH3:7])[C:21]3[C:16]([S:15][C:14]=2[CH:13]=1)=[CH:17][C:18]([CH:3]=[O:4])=[CH:19][CH:20]=3)=[O:28]

Participants

8

Reactant 4

HCID 6228DimethylformamideHCID 10340Sodium CarbonateHCID 24813Phosphorus oxychlorideHCID 219178N-Ethylphenothiazine

Product 1

HCID 15868592HCID 15868592, compound

Reagents, catalysts & solvents 3

HCID 3007855ZincchlorideCatalystHCID 962WaterSolventHCID 1140TolueneSolvent

Conditions

Temperature
80 °C

Procedure

To a mixture of 6.5 g (47.7 mmol) of dehydrated zinc chloride and 150 ml of toluene were added 14 ml (180.1 mmol) of N,N-dimethylformamide (DMF) and 10.0 g (44.0 mmol) of 10-ethylphenothiazine (4a). Thereto was gradually added dropwise 27.0 g (176.1 mmol) of phosphorus oxychloride at room temperature to 35° C. The resultant mixture was reacted at 73 to 78° C. for 3 days and then poured into 200 ml of water. This mixture was neutralized with sodium carbonate, stirred at 80° C. for 3 hours, and then subjected to liquid separation. The aqueous layer was extracted with ethyl acetate three times, and the resultant organic layer collected was dried with magnesium sulfate and concentrated. The residue was recrystallized from an isopropanol/ethyl acetate mixed solvent to obtain 4.96 g of 3,7-diformyl-10-ethylphenothiazine (2a).

Workup

  1. customsubjected to liquid separation
  2. extractionThe aqueous layer was extracted with ethyl acetate three times
  3. customthe resultant organic layer collected
  4. dry with materialwas dried with magnesium sulfate
  5. concentrationconcentrated
  6. customThe residue was recrystallized from an isopropanol/ethyl acetate mixed solvent

Sources & evidence

ORD record
ord-aed77c68688341a69f2d8f17d92c17a9
Source dataset
uspto-grants-2000_07
Patent number
US06083651

Reaction notes

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