Triethylamine → HCID 14390522, compound

HRID 2072929Notes

Reaction equation

HRID 2072929 reaction equation
Cl[C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1.Cl.[CH3:12][O:13][C:14](=[O:18])[C@@H:15]([CH3:17])[NH2:16].C(N(CC)CC)C>CO>[CH3:12][O:13][C:14](=[O:18])[C@@H:15]([CH3:17])[NH:16][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1

Participants

5

Procedure

A suspension of 2-chloro-3-nitropyridine (37.76 g, 0.239 mole), (R)-alanine methyl ester hydrochloride (50 g, 0.358 mole) and triethylamine (60.3 g, 0.597 mole) in methanol (370 ml) was refluxed overnight under nitrogen. The solvents were removed under reduced pressure and the resulting solid was triturated in ethyl acetate (300 ml), filtered, and rinsed with additional ethyl acetate. The filtrate and washings were combined and washed once with water. The aqueous wash was extracted with ethyl acetate and the combined organic layers were washed several times with water, dried over sodium sulfate, filtered and evaporated under reduced pressure to given an oil weighing 45.6 g (85%). Elution of a portion of the oil with 1:6 tetrahydrofuran/hexane through a silica gel column gave 3.2 g of product after evaporation of solvent. Drying of a portion of the solid under high vacuum at room temperature gave 0.98 g of title compound, mp 39°-40° C.

Workup

  1. temperaturewas refluxed overnight under nitrogen
  2. customThe solvents were removed under reduced pressure
  3. customthe resulting solid was triturated in ethyl acetate (300 ml)
  4. filtrationfiltered
  5. washrinsed with additional ethyl acetate
  6. washwashed once with water
  7. washThe aqueous wash
  8. extractionwas extracted with ethyl acetate
  9. washthe combined organic layers were washed several times with water
  10. dry with materialdried over sodium sulfate
  11. filtrationfiltered
  12. customevaporated under reduced pressure
  13. washElution of a portion of the oil with 1:6 tetrahydrofuran/hexane through a silica gel column

Sources & evidence

ORD record
ord-8a1c52d543744ad49746d728d9da9ddd
Source dataset
uspto-grants-1990_04
Patent number
US04914109

Reaction notes

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