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Methylamine → HCID 86674501, compound

HRID 2042808
Notes
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Reaction equation

HRID 2042808 reaction equation
[CH3:1][NH2:2].[CH3:3][O:4][C:5](=[O:21])[C:6]1[CH:11]=[C:10]([N+:12]([O-:14])=[O:13])[C:9](Cl)=[N:8][C:7]=1[O:16][CH2:17][CH:18]([F:20])[F:19]>C1COCC1>[CH3:3][O:4][C:5](=[O:21])[C:6]1[CH:11]=[C:10]([N+:12]([O-:14])=[O:13])[C:9]([NH:2][CH3:1])=[N:8][C:7]=1[O:16][CH2:17][CH:18]([F:20])[F:19]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 6329MethylamineHCID 86669290HCID 86669290, compound

Product 1

HCID 86674501HCID 86674501, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

Methylamine (2 M in THF; 32.0 mL, 64.0 mmol) is added at 10° C. to 6-chloro-2-(2,2-difluoro-ethoxy)-5-nitro-nicotinic acid methyl ester (9.1 g, 30.7 mmol) in THF (50 mL). After 1 h at rt the reaction mixture is concentrated, treated with water and filtered. The filtercake is washed with water and dried to give the sub-title compound.

Workup

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
concentration
After 1 h at rt the reaction mixture is concentrated
  • additiontreated with water
  • filtrationfiltered
  • washThe filtercake is washed with water
  • customdried
  • Sources & evidence

    ORD record
    ord-35dad638b6824fd2a5c47b5d9eb59c03
    Source dataset
    uspto-grants-2013_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08586604B2

    Reaction notes

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