反応 #2195519

ord-4f52b6d0dc2f4b309947f09c1be5ef42

反応方程式

O=c1[nH]c2ccc(Br)cc2c2ncnn12
9-bromo-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-one
[Na+].[OH-]
NaOH
Nc1ccc(Br)cc1-c1ncn[nH]1
title compound
収率 87.0%
Nc1ccc(Br)cc1-c1ncn[nH]1
4-Bromo-2-(2H-[1,2,4]triazol-3-yl)-phenylamine
収率 87.0%

反応条件

温度
140°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The resulting solution was cooled to 27° C.
  2. 2
    その他to crystallize
  3. 3
    workup.ADDITIONWater (146 mL) and 1-octanol (1.73 mL) were added
  4. 4
    workup.ADDITIONthe pH of the suspension was adjusted to 6.5 by the slow addition of glacial acetic acid (14 mL)
  5. 5
    ろ過the solid was collected by filtration
  6. 6
    洗浄washed with water and 2-propanol
  7. 7
    その他Drying in vacuo

実験手順

To a well stirred slurry of 9-bromo-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-one (32.0 g, 171 mmol) in ethylene glycol (146 mL) which was heated at 100° C., was added aq NaOH 32% (22.4 mL, 241 mmol). The slurry was heated at 140° C. for 17.5 h. The resulting solution was cooled to 27° C. and the product began to crystallize. Water (146 mL) and 1-octanol (1.73 mL) were added and the pH of the suspension was adjusted to 6.5 by the slow addition of glacial acetic acid (14 mL). The resulting slurry was stirred for 30 min, the solid was collected by filtration and washed with water and 2-propanol. Drying in vacuo afforded the title compound (25.2 g, 87%) as a light yellow solid. MS: m/e=239.0/241.1 (M+H+).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07514426B2uspto-grants-2009_04