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Ethyl Acetate → HCID 58387955, compound

HRID 2079953
Notes
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Reaction equation

HRID 2079953 reaction equation
[CH3:1][O:2][C:3](=[O:16])[C:4]1[CH:9]=[CH:8][C:7]([CH:10]=[CH:11][O:12]CC)=[N:6][C:5]=1[NH2:15].C(=O)(O)[O-].[Na+].[BH4-].[Na+].C(OCC)(=O)C>Cl.C(O)C.O1CCCC1>[CH3:1][O:2][C:3](=[O:16])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH2:11][OH:12])=[N:6][C:5]=1[NH2:15]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 4

HCID 8857Ethyl AcetateHCID 516892Sodium BicarbonateHCID 4311764Sodium borohydrideHCID 67119555HCID 67119555, compound

Product 1

HCID 58387955HCID 58387955, compoundYield 40%

Reagents, catalysts & solvents 3

HCID 313
Hydrochloric Acid
Solvent
HCID 702EthanolSolvent
HCID 8028TetrahydrofuranSolvent

Procedure

2-Amino-6-(2-ethoxy-vinyl)-nicotinic acid methyl ester (1.07 g, 4.81 mmol) was dissolved in 5N-hydrochloric acid (25 mL), ethanol (20 mL) and tetrahydrofuran (5 mL), and the solution was stirred for 3 hours under reflux. This reaction mixture was allowed to room temperature, and neutralized with a aqueous solution of saturated sodium bicarbonate, then, sodium borohydride (1 g, 26.5 mmol) was added to this reaction mixture, which was then stirred for 20 minutes at room temperature. Ethyl acetate was added thereto, followed by filtrating through Celite pad. This filtrate was partitioned. This organic layer was separated, the solvent was evaporated in vacuo, the residue was purified by silica gel column chromatography, and the title compound (350 mg, 1.92 mmol, 40%) was obtained as a brown oil.

Workup

  1. temperatureunder reflux
  2. customwas allowed to room temperature
  3. stirringwas then stirred for 20 minutes at room temperature
  4. filtrationby filtrating through Celite pad
  5. customThis filtrate was partitioned
  6. customThis organic layer was separated
  7. customthe solvent was evaporated in vacuo
  8. customthe residue was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-7303963a86174f958ed1843efbb8f200
Source dataset
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07932272B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes