Water → HCID 21913056, compound

HRID 1352605Notes

Reaction equation

HRID 1352605 reaction equation
[CH3:1][C:2]1[C:7]([CH3:8])=[C:6]([NH:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14]O)[C:5]([N+:16]([O-:18])=[O:17])=[C:4]([O:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[N:3]=1.S(Cl)([Cl:28])=O.O.C(=O)(O)[O-].[Na+]>ClCCl>[Cl:28][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][NH:9][C:6]1[C:5]([N+:16]([O-:18])=[O:17])=[C:4]([O:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[N:3]=[C:2]([CH3:1])[C:7]=1[CH3:8]

Participants

6

Reactant 4

HCID 962WaterHCID 24386Thionyl ChlorideHCID 516892Sodium BicarbonateHCID 21913716HCID 21913716, compound

Product 1

HCID 21913056HCID 21913056, compoundYield 96.2%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Conditions

Temperature
0 °C

Procedure

Under a nitrogen atmosphere, a solution of 5-(2,3-dimethyl-5-nitro-6-phenoxy-pyridin-4-ylamino)pentan-1-ol (40.24 g, 114.6 mmol) in dichloromethane (350 mL) was cooled to 0° C. Thionyl chloride (12.5 mL, 172 mmol) was added dropwise, and the reaction was heated at reflux for one hour. The reaction was cooled to 0° C., and water (200 mL) was slowly added followed by solid sodium bicarbonate until the pH of the solution was basic. The solvent was partially removed under reduced pressure, and the aqueous solution was extracted with ethyl acetate (500 mL). The combined organic solutions washed with saturated aqueous sodium bicarbonate (3×50 mL), water (1×50 mL), and brine (2×20 mL), and then dried over magnesium sulfate, filtered, and concentrated under reduced pressure to afford a yellow oil, which crystallized overnight. The solid was dried for one hour in a vacuum oven at 70° C. to provide 40.1 g of (5-chloropentyl)-(2,3-dimethyl-5-nitro-6-phenoxy-pyridin-4-yl)amine as a yellow solid.

Workup

  1. temperaturethe reaction was heated
  2. temperatureat reflux for one hour
  3. customThe solvent was partially removed under reduced pressure
  4. extractionthe aqueous solution was extracted with ethyl acetate (500 mL)
  5. washThe combined organic solutions washed with saturated aqueous sodium bicarbonate (3×50 mL), water (1×50 mL), and brine (2×20 mL)
  6. dry with materialdried over magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customto afford a yellow oil, which
  10. customcrystallized overnight
  11. customThe solid was dried for one hour in a vacuum oven at 70° C.

Sources & evidence

ORD record
ord-7128f998eae843fd953c7e7064ff52b9
Source dataset
uspto-grants-2007_05
Patent number
US07220758B2

Reaction notes

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