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Tetrahydrofuran → HCID 86669311, compound

HRID 450338
Notes
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Reaction equation

HRID 450338 reaction equation
C[O:2][C:3](=[O:20])[C:4]1[CH:9]=[C:8]([N+:10]([O-:12])=[O:11])[C:7]([NH:13]C)=[N:6][C:5]=1[O:15][CH2:16][CH:17]([F:19])[F:18].C1COCC1.[OH-].[Na+]>O>[F:19][CH:17]([F:18])[CH2:16][O:15][C:5]1[N:6]=[C:7]([NH2:13])[C:8]([N+:10]([O-:12])=[O:11])=[CH:9][C:4]=1[C:3]([OH:20])=[O:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 8028TetrahydrofuranHCID 14798Sodium HydroxideHCID 86674501HCID 86674501, compound

Product 1

HCID 86669311HCID 86669311, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

A mixture of methyl-2-(2,2-difluoro-ethoxy)-6-methylamino-5-nitro-nicotinate (9.1 g, 32 mmol, prepared according to WO2010/34799), THF (100 mL), water (60 mL) and 1N aq. NaOH-solution (60 mL) is stirred for 3 h at rt, then the mixture is concentrated i.vac. The water phase is washed with Et2O, 60 mL 1N HCl solution is added and the resulting precipitate is collected and dried.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. concentrationthe mixture is concentrated i.vac
  2. washThe water phase is washed with Et2O, 60 mL 1N HCl solution
  3. additionis added
  4. customthe resulting precipitate is collected
  5. customdried

Sources & evidence

ORD record
ord-78e8eb5b6896447289695f792af65301
Source dataset
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08486968B2

Reaction notes

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