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Sodium Azide → 4-Aminosampangine

HRID 483839
ノート
印刷プレビュー

反応式

HRID 483839 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 33557Sodium AzideHCID 99048014-Bromosampangine

生成物 1

HCID 117767144-Aminosampangine収率 91%

試薬・触媒・溶媒 2

HCID 180Acetone溶媒HCID 962Water溶媒

反応条件

温度
10 °C

実験手順

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%).

後処理

  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

出典と根拠

ORDレコード
ord-5aaeb16a297043e0af1a31cdca21d72f
出典データセット
uspto-grants-1993_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05227383

反応ノート

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