反応 #1688993

ord-7a5a741133fd4c48aebdea685bee7c66

反応方程式

O=C(O)CCCO
4-hydroxybutyric acid
Nc1cccnc1N
2,3-diaminopyridine
Cl
hydrochloric acid
N
ammonia
OCCCc1nc2cccnc2[nH]1
title compound
収率 66.4%
OCCCc1nc2cccnc2[nH]1
2-(3-Hydroxypropyl)-3H-imidazo[4,5-b]pyridine
収率 66.4%

反応条件

温度
150°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The aqueous mixture was evaporated to dryness under reduced pressure
  2. 2
    その他the resulting residue was purified by column chromatography through silica gel
  3. 3
    workup.ADDITIONby volume mixture of ethyl acetate and methanol as the eluent
  4. 4
    その他The product was crystallized by trituration with ethyl acetate

実験手順

0.83 g of 4-hydroxybutyric acid (prepared as described in Preparation 32) was added to 0.77 g of 2,3-diaminopyridine, and the resulting mixture was stirred at 150° C. for 4 hours. At the end of this time, the reaction mixture was treated with 3 N aqueous hydrochloric acid and subsequently made alkaline by the addition of aqueous ammonia. The aqueous mixture was evaporated to dryness under reduced pressure, and then the resulting residue was purified by column chromatography through silica gel, using a 5:1 by volume mixture of ethyl acetate and methanol as the eluent. The product was crystallized by trituration with ethyl acetate, to give 0.83 g of the title compound, melting at 151-153° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05977365uspto-grants-1999_11