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

Tetrahydrofuran → HCID 67230022, compound

HRID 1410192
Notes
Print preview

Reaction equation

HRID 1410192 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:17]=[CH:18][C:19]=1[NH:20][CH3:21])[C:7]([NH:9][C:10]1[CH:15]=[CH:14][C:13]([Br:16])=[CH:12][CH:11]=1)=[O:8])([O-])=O.C1COCC1>CO>[NH2:1][C:4]1[CH:5]=[C:6]([CH:17]=[CH:18][C:19]=1[NH:20][CH3:21])[C:7]([NH:9][C:10]1[CH:11]=[CH:12][C:13]([Br:16])=[CH:14][CH:15]=1)=[O:8]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 8028TetrahydrofuranHCID 7406921HCID 7406921, compound

Product 1

HCID 67230022HCID 67230022, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

A mixture of 3-Nitro-N-(4-bromophenyl)-4-methylaminobenzamide (120 mg, 0.34 mmol), 10 ml THF, 10 ml MeOH and 30 mg 5%-Pt-on-carbon was stirred for 4 h under a hydrogen atmosphere (3.5 bar). The catalyst was removed by filtration and the mixture was concentrated and used in the next step without further purification.

Workup

  1. customThe catalyst was removed by filtration
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
  • concentrationthe mixture was concentrated
  • customused in the next step without further purification
  • Sources & evidence

    ORD record
    ord-6bcec334eb1f4c9099e025f4351ea38b
    Source dataset
    uspto-grants-2014_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08921405B2

    Reaction notes

    Loading…