HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

HCID 66742608, compound → 5-(4-Methylpiperazin-1-YL)pyrazin-2-amine

HRID 449634
Notes
Print preview

Reaction equation

HRID 449634 reaction equation
[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([C:8]2[CH:13]=[N:12][C:11]([N+:14]([O-])=O)=[CH:10][N:9]=2)[CH2:4][CH2:3]1>CO.[Pd]>[CH3:1][N:2]1[CH2:3][CH2:4][N:5]([C:8]2[CH:13]=[N:12][C:11]([NH2:14])=[CH:10][N:9]=2)[CH2:6][CH2:7]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 1

HCID 66742608HCID 66742608, compound

Product 1

HCID 592999765-(4-Methylpiperazin-1-YL)pyrazin-2-amineYield 98.6%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 887MethanolSolvent

Procedure

2-(4-methylpiperazin-1-yl)-5-nitropyrazine (328 mg, 1.47 mmol) was dissolved in MeOH (15 ml) at room temperature. Pd/C (10%) (50 mg) was added while the reaction mixture was stirred. The reaction mixture was placed under a H2 balloon and stirred at rt for 1.5 hrs. The reaction mixture was filtered through celite and washed with MeOH (30 mL). The filtrate was stripped and dried under vacuum after azeotroping with toluene twice to give a light brown gummy material (280 mg, yield 89%).

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. stirringstirred at rt for 1.5 hrs
  2. filtrationThe reaction mixture was filtered through celite
  3. washwashed with MeOH (30 mL)
  4. customdried under vacuum
  5. customafter azeotroping with toluene twice

Sources & evidence

ORD record
ord-b591a05082434a8e9fc939d53a9b051d
Source dataset
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08481540B2

Reaction notes

Loading…