Sulfuric Acid → methyl 6-amino-2,3-dihydro-1H-benzo[d]pyrrolo[1,2-a]imidazole-5-carboxylate

HRID 715986Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 715986
CC(C)(C)C([NH:5][C:6]1[C:17]([C:18]([O:20][CH3:21])=[O:19])=[C:10]2[N:11]=[C:12]3[CH2:16][CH2:15][CH2:14][N:13]3[C:9]2=[CH:8][CH:7]=1)=O.S(=O)(=O)(O)O>CO>[NH2:5][C:6]1[C:17]([C:18]([O:20][CH3:21])=[O:19])=[C:10]2[N:11]=[C:12]3[CH2:16][CH2:15][CH2:14][N:13]3[C:9]2=[CH:8][CH:7]=1

Komponenten

4

Versuchsvorschrift

A solution of methyl 6-(2,2-dimethylpropionylamino)-2,3-dihydro-1Hbenzo[d]pyrrolo[1,2-a]imidazole-5-carboxylate (Intermediate 56, 0.61 g) and concentrated sulfuric acid (1.5 mL) in methanol (30 mL) was stirred and heated at reflux for 44 hours. After cooling, the solution was concentrated in vacuo and the residue was dissolved in water and ethyl acetate and basified with 5M sodium hydroxide solution. The aqueous phase was extracted with ethyl acetate (×8) and the combined extracts were dried (Na2SO4) and filtered. The filtrate was concentrated in vacuo and the residue was triturated with ether and filtered to give methyl 6-amino-2,3-dihydro-1H-benzo[d]pyrrolo[1,2-a]imidazole-5-carboxylate (0.296 g) as an off-white solid.

Aufarbeitung

  1. temperatureheated
  2. temperatureat reflux for 44 hours
  3. temperatureAfter cooling
  4. concentrationthe solution was concentrated in vacuo
  5. dissolutionthe residue was dissolved in water
  6. extractionThe aqueous phase was extracted with ethyl acetate (×8)
  7. dry with materialthe combined extracts were dried (Na2SO4)
  8. filtrationfiltered
  9. concentrationThe filtrate was concentrated in vacuo
  10. customthe residue was triturated with ether
  11. filtrationfiltered

Quellen und Nachweise

ORD-Eintrag
ord-12b7980aee334d7991cb4dd5ba7871ec
Quelldatensatz
uspto-grants-2015_11
Patentnummer
US09187494B2

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