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Piperazine → 1-[6-Methyl-4-(trifluoromethyl)pyridin-2-yl]piperazine

HRID 1044606
Notes
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Reaction equation

HRID 1044606 reaction equation
Cl[C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[C:4]([CH3:12])[N:3]=1.[NH:13]1[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]1.C(N(CC)CC)C>O1CCOCC1.O>[CH3:12][C:4]1[N:3]=[C:2]([N:13]2[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]2)[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 4837PiperazineHCID 8471TriethylamineHCID 27366262-Chloro-6-methyl-4-(trifluoromethyl)pyridine

Product 1

HCID 598335501-[6-Methyl-4-(trifluoromethyl)pyridin-2-yl]piperazineYield 70.2%

Reagents, catalysts & solvents 2

HCID 962WaterSolvent
HCID 31275
1,4-Dioxane
Solvent

Conditions

Temperature
100 °C

Procedure

A solution of 2-chloro-6-methyl-4-(trifluoromethyl)pyridine (1.0 g, 5.11 mmol), piperazine (1.32 g, 15.3 mmol), and triethylamine (0.71 mL, 5.1 mmol) were mixed in 1,4-dioxane (10 mL). After stirring at 100° C. for 5 h, the reaction solution was diluted with water and extracted with ethyl acetate three times, dried with sodium sulfate, filtered, and concentrated in vacuo. The crude residue was purified by flash column chromatography (10% MeOH/5% Et3N/EtOAc) to yield the desired product (880 mg, 70.2%). LCMS calculated for C11H15F3N3: (M+H) 246.1; found 246.1.

Workup

  1. extractionextracted with ethyl acetate three times
  2. dry with materialdried with sodium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. customThe crude residue was purified by flash column chromatography (10% MeOH/5% Et3N/EtOAc)

Sources & evidence

ORD record
ord-963f294fa01d4ce694537e45b8b8e66a
Source dataset
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08563582B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes