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Sodium Azide → 4-Aminosampangine

HRID 483839
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HRID 483839 반응식
[CH:1]1[CH:6]=[C:5]2[C:7]3[C:12]4[C:13]([C:18](=[O:19])[C:4]2=[CH:3][CH:2]=1)=[N:14][CH:15]=[C:16](Br)[C:11]=4[CH:10]=[CH:9][N:8]=3.[N-:20]=[N+]=[N-].[Na+]>CC(C)=O.O>[CH:1]1[CH:6]=[C:5]2[C:7]3[C:12]4[C:13]([C:18](=[O:19])[C:4]2=[CH:3][CH:2]=1)=[N:14][CH:15]=[C:16]([NH2:20])[C:11]=4[CH:10]=[CH:9][N:8]=3
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 33557Sodium AzideHCID 99048014-Bromosampangine

생성물 1

HCID 117767144-Aminosampangine수율 91%

시약·촉매·용매 2

HCID 180Acetone용매HCID 962Water용매

반응 조건

온도
10 °C

실험 절차

A mixture of 4-bromosampangine (622 mg, 2.0 mmol) in acetone (40 mL) and sodium azide (1.30 g, 20.0 mmol) in H2O (10 mL) was heated at reflux for 1 h. The acetone was then removed by evaporation, MeOH (40 mL) added, and the mixture transferred to a three necked flask and cooled to 10° C. Piperidine (2 drops) was added and a stream of hydrogen sulfide bubbled through the reaction. After 30 min, the temperature was allowed to rise to 23° C. and the reaction continued for an additional 30 min. The solvent was then removed evaporated and the residue chromatographed as above to give 4-aminosampangine (23) (450 mg, 91%).

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 1 h
  3. customThe acetone was then removed by evaporation, MeOH (40 mL)
  4. additionadded
  5. additionPiperidine (2 drops) was added
  6. customa stream of hydrogen sulfide bubbled through the reaction
  7. customto rise to 23° C.
  8. waitthe reaction continued for an additional 30 min
  9. customThe solvent was then removed
  10. customevaporated
  11. customthe residue chromatographed as above

출처 및 근거

ORD 기록
ord-5aaeb16a297043e0af1a31cdca21d72f
출처 데이터셋
uspto-grants-1993_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05227383

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