Piperazine → HCID 22418728, compound

HRID 1682349Notes

Reaction equation

HRID 1682349 reaction equation
[CH2:1]([N:3]([CH2:12][CH3:13])[C:4]1[N:9]=[C:8]([Cl:10])[CH:7]=[C:6](Cl)[N:5]=1)[CH3:2].[NH:14]1[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]1>C(O)C>[CH2:12]([N:3]([CH2:1][CH3:2])[C:4]1[N:5]=[C:6]([N:14]2[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]2)[CH:7]=[C:8]([Cl:10])[N:9]=1)[CH3:13]

Participants

4

Reactant 2

HCID 4837PiperazineHCID 22418747HCID 22418747, compound

Product 1

HCID 22418728HCID 22418728, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

2-Diethylamino-4,6-dichloropyrimidine (10 g) is reacted with piperazine (14.45 g) in ethanol (200 ml) at reflux for 2 hr. The mixture is concentrated and the product isolated by silica gel chromatography giving 2-diethylamino-4-piperazino-6-chloropyrimidine. The 2-diethylamino-4-piperazino-6-chloropyrimidine (8 g) and N-methylpiperazine (8 g) is heated neat at 70° for 16 hr. Then water (2.5 ml) is added and the mixture is heated at 100° for 50 hr. The mixture is chromatrographed on silica gel, the appropriate fractions are pooled and concentrated to give the title compound, NMR (CDCl3) 1.15, 2.80, 2.85, 2.90, 3.30, 3.70 and 4.95 δ.

Workup

  1. temperatureat reflux for 2 hr
  2. concentrationThe mixture is concentrated
  3. customthe product isolated by silica gel chromatography

Sources & evidence

ORD record
ord-fdb1abfd41534a579caa478ccb4f328c
Source dataset
uspto-grants-1992_12
Patent number
US05175281

Reaction notes

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