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Diisopropylethylamine → 3-((2R,6S)-2,6-dimethylmorpholino)-5-fluoropicolinic acid

HRID 245374
Notes
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Reaction equation

HRID 245374 reaction equation
F[C:2]1[C:3]([C:9]([OH:11])=[O:10])=[N:4][CH:5]=[C:6]([F:8])[CH:7]=1.[CH3:12][C@H:13]1[O:18][C@@H:17]([CH3:19])[CH2:16][NH:15][CH2:14]1.CCN(C(C)C)C(C)C>C1COCC1.CCOC(C)=O>[CH3:19][C@@H:17]1[CH2:16][N:15]([C:2]2[C:3]([C:9]([OH:11])=[O:10])=[N:4][CH:5]=[C:6]([F:8])[CH:7]=2)[CH2:14][C@H:13]([CH3:12])[O:18]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 81531DiisopropylethylamineHCID 6415002,6-Dimethylmorpholine, cis-HCID 27832623,5-Difluoropyridine-2-carboxylic acid

Product 1

HCID 673194173-((2R,6S)-2,6-dimethylmorpholino)-5-fluoropicolinic acidYield 102.2%

Reagents, catalysts & solvents 2

HCID 8028TetrahydrofuranSolvent
HCID 8857
Ethyl Acetate
Solvent

Procedure

A solution of 3,5-difluoropicolinic acid (20.5 g, 128.86 mmol), cis-2,6-dimethylmorpholine (63.5 ml, 515.43 mmol) and DIEA (45.0 ml, 257.72 mmol) in THF (200 ml) was stirred at room temperature for 3 days. The mixture was diluted with EtOAc and extracted 3 times with aqueous Na2CO3. The aqueous layer was acidified with 1N HCl to bring pH to about 3 and was then saturated with NaCl before being extracted 10 times with EtOAc. The EtOAc layers were dried (MgSO4) and solvent was removed to give 33.5 g of product as a solid.

Workup

  1. extractionextracted 3 times with aqueous Na2CO3
  2. extractionsaturated with NaCl before being extracted 10 times with EtOAc
  3. dry with materialThe EtOAc layers were dried (MgSO4) and solvent
  4. customwas removed

Sources & evidence

ORD record
ord-6144bb6c74bc472fad7fe332aca65051
Source dataset
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08658641B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes