반응 #1009

ord-6c6336c7aeca4c6480e93df00f4ca622

반응 방정식

CNc1ccnc(Cl)c1N
3-amino-2-chloro-4-methylaminopyridine
CCOC(OCC)OCC
triethyl orthoformate
Cn1cnc2c(Cl)nccc21
4-chloro-1-methyl-1H-imidazo[4,5-c]pyridine
수율 91.1%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.DISTILLATIONA short path distillation apparatus
  2. 2
    기타The reaction flask was lowered into a hot oil bath
  3. 3
    온도The time spent heating
  4. 4
    온도On cooling
  5. 5
    workup.DISSOLUTIONthe thick residue was dissolved in CH2Cl2 (40 mL)
  6. 6
    workup.STIRRINGto stir overnight with a little CaO
  7. 7
    기타The solid was removed by filtration
  8. 8
    농축the filtrate was concentrated

실험 절차

To a heterogeneous mixture of 3-amino-2-chloro-4-methylaminopyridine (5.9 g, 37 mmol) and triethyl orthoformate (12.92 mL, 87.2 mmol) was added 5 drops of conc. H2SO4. A short path distillation apparatus was attached. The reaction flask was lowered into a hot oil bath and stirred at 110° C. to 190° C. The time spent heating was 20-25 minutes. On cooling, the thick residue was dissolved in CH2Cl2 (40 mL) and was allowed to stir overnight with a little CaO. The solid was removed by filtration and the filtrate was concentrated. Flash chromatography on silica gel eluting with (CH2Cl2 /CH3OH, 95:5) gave 5.65 g (91%) of 4-chloro-1-methyl-1H-imidazo[4,5-c]pyridine as a light yellow solid: mp 127°-131° C.; MS 167 (M+).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723468uspto-grants-1998_03