반응 #319216

ord-3bcb2be2d0514a2dbfe62c58f6c9a0af

반응 방정식

Cc1nc2cnccc2[nH]1
2-Methylimidazo[4,5-c]pyridine
O=C1OCCO1
ethylene carbonate
Cc1nc2ccncc2n1CCO
title compound
수율 9.0%
Cc1nc2ccncc2n1CCO
3-(2-Hydroxyethyl)-2-methylimidazo[4,5-c]pyridine
수율 9.0%

반응 조건

온도
150°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The crude black product was chromatographed on silica eluting with 40% methanol in ethyl acetate
  2. 2
    기타The fraction with Rf 0.33 in methanol, ethyl acetate, (2:3) was evaporated
  3. 3
    workup.ADDITIONwas identified as a mixture of the title compound and of the isomeric 1-(2-hydroxyethyl)-2-methylimidazo[4,5-c]pyridine
  4. 4
    기타The mixture was chromatographed on silica eluting with 20% methanol in acetone
  5. 5
    workup.ADDITIONFractions containing the more mobile isomer
  6. 6
    기타evaporated

실험 절차

2-Methylimidazo[4,5-c]pyridine (10.6 g) was mixed with ethylene carbonate (8.3 g) and heated as a melt at 150° C. for 1/2 hour. The crude black product was chromatographed on silica eluting with 40% methanol in ethyl acetate. The fraction with Rf 0.33 in methanol, ethyl acetate, (2:3) was evaporated and was identified as a mixture of the title compound and of the isomeric 1-(2-hydroxyethyl)-2-methylimidazo[4,5-c]pyridine. The mixture was chromatographed on silica eluting with 20% methanol in acetone. Fractions containing the more mobile isomer were combined and evaporated yielding the title compound (1.22 g, 9%) as a foam.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04851412uspto-grants-1989_07