Piperidine → 6-Piperidin-1-yl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine

HRID 217674노트

반응식

HRID 217674 반응식
Br.Cl[C:3]1[CH:4]=[CH:5][C:6]2[N:7]([C:9]([NH2:12])=[N:10][N:11]=2)[N:8]=1.[NH:13]1[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1>O>[N:13]1([C:3]2[CH:4]=[CH:5][C:6]3[N:7]([C:9]([NH2:12])=[N:10][N:11]=3)[N:8]=2)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1

참가 물질

4

실험 절차

6-Chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine hydrobromide (W2.001; 100 mg) were initially charged in water (1 ml) and admixed with piperidine (260 μl) with stirring. Thereafter, the mixture was heated to reflux for 1 h and, after cooling, freed of the solvent. Subsequently, the mixture was admixed with water and the solid formed was filtered off with suction and dried. The mother liquor was dried and admixed with a little water. The solid obtained was filtered off with suction and dried. The filtrate was then extracted three times with dichloromethane. The combined organic phases were dried over sodium sulfate and, after the desiccant had been filtered off, dried under reduced pressure. The three resulting solid fractions were combined and gave rise to 56 mg of the title compound.

후처리

  1. temperatureThereafter, the mixture was heated
  2. temperatureto reflux for 1 h
  3. temperatureafter cooling, freed of the solvent
  4. customthe solid formed
  5. filtrationwas filtered off with suction
  6. customdried
  7. customThe mother liquor was dried
  8. customThe solid obtained
  9. filtrationwas filtered off with suction
  10. customdried
  11. extractionThe filtrate was then extracted three times with dichloromethane
  12. dry with materialThe combined organic phases were dried over sodium sulfate
  13. filtrationafter the desiccant had been filtered off
  14. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-54e1cb8527cf46c4896cfb1e2f9d958f
출처 데이터셋
uspto-grants-2012_06
특허 번호
US08198272B2

반응 노트

불러오는 중…