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Bromine → 1-(5-Bromopyrimidin-2-yl)piperazine

HRID 981983
Notes
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Reaction equation

HRID 981983 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[N:3][C:2]=1[N:7]1[CH2:12][CH2:11][NH:10][CH2:9][CH2:8]1.[Br:13]Br>Cl>[Br:13][C:5]1[CH:6]=[N:1][C:2]([N:7]2[CH2:12][CH2:11][NH:10][CH2:9][CH2:8]2)=[N:3][CH:4]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 24408BromineHCID 887471-(2-Pyrimidinyl)piperazine

Product 1

HCID 27571751-(5-Bromopyrimidin-2-yl)piperazineYield 62%

Reagents, catalysts & solvents 1

HCID 313Hydrochloric AcidSolvent

Conditions

Temperature
100 °C

Procedure

To an ice-cooled solution of 1-(2-pyrimidinyl) piperazine (16.4 g, 0.1 mole) in 1N HCl (100 mL) was added dropwise bromine (15.98 g, 0.1 mole). After stirring at 0° for 0.5 h. the mixture was heated to 100° C. until dissipation of the red color had occurred. The mixture was filtered, cooled, made alkaline with 50% NaOH and extracted with Et2O. The dried extract (MgSO4) was concentrated in vacuo to provide 14.5 g (62%) of product, m.p. 73°-75° C.

Workup

  1. filtrationThe mixture was filtered
  2. temperaturecooled
  3. extractionextracted with Et2O
  4. extractionThe dried extract (MgSO4)
  5. concentrationwas concentrated in vacuo

Sources & evidence

ORD record
ord-d8d10a631f5f401f901c9bb0859e0d45
Source dataset
uspto-grants-1991_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04994460

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes