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

HCID 12535827, compound → HCID 12535828, compound

HRID 2082734
Notes
Print preview

Reaction equation

HRID 2082734 reaction equation
[O:1]=[C:2]1[NH:7][C:6]([C:8]2[CH:13]=[C:12]([N+:14]([O-])=O)[CH:11]=[CH:10][C:9]=2[O:17][CH2:18][CH3:19])=[N:5][CH:4]=[C:3]1[C:20]([O:22][CH2:23][CH3:24])=[O:21].[H][H]>[Pd].C(O)C>[O:1]=[C:2]1[NH:7][C:6]([C:8]2[CH:13]=[C:12]([NH2:14])[CH:11]=[CH:10][C:9]=2[O:17][CH2:18][CH3:19])=[N:5][CH:4]=[C:3]1[C:20]([O:22][CH2:23][CH3:24])=[O:21]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 12535827HCID 12535827, compoundHCID 178418361HCID 178418361, compound2×

Product 1

HCID 12535828HCID 12535828, compoundYield 31.6%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 702EthanolSolvent

Procedure

A mixture of ethyl 1,6-dihydro-6-oxo-2-(2-ethoxy-5- nitrophenyl)pyrimidine-5-carboxylate (0.42 g., 1.26 mmoles) and 10% palladium on carbon (0.07 g.) in ethanol (200 ml.) was treated with hydrogen at a pressure of about 3.5 kg./cm2 until uptake of hydrogen ceased. The mixture was filtered and the filtrate reduced to dryness. The residue was recrystallized from water followed by aqueous ethanol to give the title compound (0.12 g., 31.6%), m.p. 107°-110°.

Workup

  1. filtrationThe mixture was filtered
  2. customThe residue was recrystallized from water

Sources & evidence

ORD record
ord-64aa315c0a924b7386afe631c9fd7970
Source dataset
uspto-grants-1978_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04082751

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes