Water → HCID 19851783, 화합물

HRID 34932노트

반응식

HRID 34932 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH3:27])[C:5]([CH2:8][CH2:9][CH2:10][N:11]2[C:15]3=[N:16][CH:17]=[C:18]([CH2:20][C:21]4[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=4)[CH:19]=[C:14]3N=N2)=[N:6][CH:7]=1.[OH2:28].[OH-].[NH4+]>C(Cl)(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]([CH3:27])[C:5]([CH2:8][CH2:9][CH2:10][NH:11][C:15]2[C:14]([OH:28])=[CH:19][C:18]([CH2:20][C:21]3[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=3)=[CH:17][N:16]=2)=[N:6][CH:7]=1

참가 물질

5

실험 절차

3-[3-(5-Bromo-3-methylpyrid-2-yl)propyl]-6-(3-pyridylmethyl)-3H-1,2,3-triazolo[5,4-b]pyridine (2.68 g) was added in portions over 15 minutes to hot (190°-200° C.) stirred polyphosphoric acid (10.45 g). The stirred reaction was heated at 190°-200° C. for a further 45 minutes, water (20 ml) was added to the hot reaction mixture, the solution was neutralised with concentrated ammonium hydroxide and allowed to cool. The pH was then raised to 10, chloroform extraction of the aqueous mixture gave a brown solid. This solid was recrystallised from ethanol/ether giving buff crystals (1.64 g). These were chromatographed on silica in methanol/chloroform 1:9, the product was then recrystallised from chloroform/petroleum ether (40°-60° C.) to give the title compound (1.4 g) (off-white crystals), m.p. 141°-143° C.

후처리

  1. customThe stirred reaction
  2. temperaturewas heated at 190°-200° C. for a further 45 minutes
  3. temperatureto cool
  4. customgave a brown solid
  5. customThis solid was recrystallised from ethanol/ether giving buff crystals (1.64 g)
  6. customThese were chromatographed on silica in methanol/chloroform 1:9
  7. customthe product was then recrystallised from chloroform/petroleum ether (40°-60° C.)

출처 및 근거

ORD 기록
ord-e01fb21c2c1144d38adac2354ac31156
출처 데이터셋
uspto-grants-1988_08
특허 번호
US04764519

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