Sodium Hydroxide → N'-[6-(2,4-Dichloro-phenoxy)-pyridin-3-yl]-N-ethyl-N-methyl-formamidine

HRID 1894652Notes

Reaction equation

HRID 1894652 reaction equation
[CH2:1]([N:3]([CH3:6])[CH:4]=O)[CH3:2].[Cl:7][C:8]1[CH:21]=[C:20]([Cl:22])[CH:19]=[CH:18][C:9]=1[O:10][C:11]1[N:16]=[CH:15][C:14]([NH2:17])=[CH:13][CH:12]=1.[OH-].[Na+]>ClCCl>[Cl:7][C:8]1[CH:21]=[C:20]([Cl:22])[CH:19]=[CH:18][C:9]=1[O:10][C:11]1[N:16]=[CH:15][C:14]([N:17]=[CH:4][N:3]([CH2:1][CH3:2])[CH3:6])=[CH:13][CH:12]=1

Participants

5

Reactant 3

HCID 14798Sodium HydroxideHCID 350667N-ethyl-N-methylformamideHCID 7357766-(2,4-Dichlorophenoxy)pyridin-3-amine

Product 1

HCID 25158514N'-[6-(2,4-Dichloro-phenoxy)-pyridin-3-yl]-N-ethyl-N-methyl-formamidineYield 48.8%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

In a 25 ml single-necked round-bottomed flask, ethylmethylformamide (350 mg) is solubilized in dry dichloromethane (4 ml) at ambient temperature (colourless solution). Under stirring phosphorous oxide chloride (0.4 ml) is added dropwise by syringe. Stirring at ambient temperature is continued for 1 hour. To this solution, 6-(2,4-Dichloro-phenoxy)-pyridin-3-ylamine (0.5 g) dissolved in 1.0 ml of dry dichloromethane is added dropwise by syringe, giving a yellow solution. Stirring is continued at an ambient temperature for 1 hour. The mixture is then poured into ice/water (pH=2, water phase). 2 M aqueous NaOH is then added to get a pH of about 11 and stirring is continued for 10 minutes. The mixture is then extracted with dichloromethane (2×50 ml). The combined organic phases are then dried over sodium sulfate, filtered and the solvent is removed in vacuo. Purification by flash chromatography over silica gel with hexane/ethyl acetate 3:4 (v:v) gives 0.31 g of the compound as a yellow oil.

Workup

  1. additionUnder stirring phosphorous oxide chloride (0.4 ml) is added dropwise by syringe
  2. additionis added dropwise by syringe
  3. customgiving a yellow solution
  4. stirringStirring
  5. waitis continued at an ambient temperature for 1 hour
  6. customto get a pH of about 11
  7. stirringstirring
  8. waitis continued for 10 minutes
  9. extractionThe mixture is then extracted with dichloromethane (2×50 ml)
  10. dry with materialThe combined organic phases are then dried over sodium sulfate
  11. filtrationfiltered
  12. customthe solvent is removed in vacuo
  13. customPurification by flash chromatography over silica gel with hexane/ethyl acetate 3:4 (v:v)

Sources & evidence

ORD record
ord-cb6d1a1ef7324a129add46e1c06154bf
Source dataset
uspto-grants-2013_08
Patent number
US08513286B2

Reaction notes

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