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

HCID 90383149, compound → 4-(4-Acetyl-piperazin-1-YL)-2-chloroaniline

HRID 1496957
Notes
Print preview

Reaction equation

HRID 1496957 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([N:11]2[CH2:16][CH2:15][N:14]([C:17](=[O:19])[CH3:18])[CH2:13][CH2:12]2)[CH:5]=[CH:6][C:7]=1[N+:8]([O-])=O>C(O)C>[NH2:8][C:7]1[CH:6]=[CH:5][C:4]([N:11]2[CH2:16][CH2:15][N:14]([C:17](=[O:19])[CH3:18])[CH2:13][CH2:12]2)=[CH:3][C:2]=1[Cl:1]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 90383149HCID 90383149, compound

Product 1

HCID 534262724-(4-Acetyl-piperazin-1-YL)-2-chloroaniline

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
90 °C

Procedure

The compound prepared in Step 1 was dissolved in ethanol (10 ml) and distilled water (1.0 ml), added with iron (powder, 2.0 g) and ammonium chloride (1.0 g), and stirred at 90° C. for 2 hours. Then, the resultant was filtered using celite and the filtrate was distilled under reduced pressure to remove the solvent. The resulting white solid was used in the subsequent reaction without further purification.

Workup

  1. distillationdistilled water (1.0 ml)
  2. additionadded with iron (powder, 2.0 g) and ammonium chloride (1.0 g)
  3. filtrationThen, the resultant was filtered
  4. distillationthe filtrate was distilled under reduced pressure
  5. customto remove the solvent
  6. customThe resulting white solid was used in the subsequent reaction without further purification

Sources & evidence

ORD record
ord-ba5414df8f934728aa66e9826a823895
Source dataset
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09199944B2

Reaction notes

Loading…

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes