Methylamine → Methyl(3-(5-(phenylmethoxy)(3-pyridyloxy))propyl)amine
Reaction equation
Cl[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:7]=[C:8]([O:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:9]=[N:10][CH:11]=1.[CH3:20][NH2:21]>CO>[CH3:20][NH:21][CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[N:10][CH:9]=[C:8]([O:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:7]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
The 5-(3-chloropropoxy)-3-(phenylmethoxy)pyridine (1.52 g, 5.49 mmol) was dissolved in methanol (25 mL) and added to a 40 wt % aqueous solution of methylamine (50 mL) in a heavy-walled glass pressure-tube apparatus. The tube was sealed and the mixture was stirred and heated at 100° C. (oil bath temperature) for 4 h. After cooling, the mixture was concentrated by rotary evaporation. Saturated NaCl solution (25 mL) was added to the residue. The pH of the solution was adjusted to 6, and impurities were extracted with ether (3×15 mL). The aqueous layer was basified to pH 10 with 100% NaOH solution and extracted with chloroform (4×15 mL). The combined chloroform extracts were dried (Na2SO4), filtered, and concentrated by rotary evaporation to a residue that was dried briefly under high vacuum to give 1.07 g (71.7%) of an oil.
Workup
- customThe tube was sealed
- temperatureAfter cooling
- concentrationthe mixture was concentrated by rotary evaporation
- additionSaturated NaCl solution (25 mL) was added to the residue
- extractionwere extracted with ether (3×15 mL)
- extractionextracted with chloroform (4×15 mL)
- dry with materialThe combined chloroform extracts were dried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated by rotary evaporation to a residue that
- customwas dried briefly under high vacuum
Sources & evidence
- ORD record
- ord-e732b8bb2c27456f962b497cda1fec6f
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06441006B2
Reaction notes
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