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Sodium Hydroxide → 4-Bromo-2-(1H-1,2,4-triazol-3-yl)aniline

HRID 2108337
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HRID 2108337 반응식
[Br:1][C:2]1[CH:11]=[CH:10][C:9]2[NH:8]C(=O)[N:6]3[N:13]=[CH:14][N:15]=[C:5]3[C:4]=2[CH:3]=1.[OH-].[Na+]>C(O)CO>[Br:1][C:2]1[CH:11]=[CH:10][C:9]([NH2:8])=[C:4]([C:5]2[NH:6][N:13]=[CH:14][N:15]=2)[CH:3]=1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 1357668559-Bromo-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one

생성물 1

HCID 620726444-Bromo-2-(1H-1,2,4-triazol-3-yl)aniline수율 87%

시약·촉매·용매 1

HCID 174Ethylene Glycol용매

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온도
140 °C

실험 절차

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+).

후처리

  1. temperatureThe resulting solution was cooled to 27° C.
  2. customto crystallize
  3. additionWater (146 mL) and 1-octanol (1.73 mL) were added
  4. additionthe pH of the suspension was adjusted to 6.5 by the slow addition of glacial acetic acid (14 mL)
  5. filtrationthe solid was collected by filtration
  6. washwashed with water and 2-propanol
  7. customDrying in vacuo

출처 및 근거

ORD 기록
ord-4f52b6d0dc2f4b309947f09c1be5ef42
출처 데이터셋
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07514426B2

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