Morpholine → HCID 59555414, compound
Reaction equation
Br[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([CH2:9][Br:10])[N:4]=1.[NH:11]1[CH2:16][CH2:15][O:14][CH2:13][CH2:12]1>C(O)C>[Br:10][CH2:9][C:5]1[N:4]=[C:3]([CH2:2][N:11]2[CH2:16][CH2:15][O:14][CH2:13][CH2:12]2)[CH:8]=[CH:7][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2,6-Bis(bromomethyl)pyridine (265 mg) was suspended in 2 mL of ethanol, thereto 87 mg of morpholine was added at ice temperature, and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and the residue was purified by chromatography on silica gel (methylene chloride-ethanol-triethylamine=400:20:1 (v/v, the same hereinafter)) to give 90 mg of 4-(6-bromomethylpyridin-2-ylmethyl)morpholine as a white powder.
Workup
- concentrationThe reaction mixture was concentrated under reduced pressure
- customthe residue was purified by chromatography on silica gel (methylene chloride-ethanol-triethylamine=400:20:1 (v/v
Sources & evidence
- ORD record
- ord-9098a6f21977425da26a8e812a48c144
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07834002B2
Reaction notes
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