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Sodium Azide → HCID 57708028、化合物

HRID 2044860
ノート
印刷プレビュー

反応式

HRID 2044860 の反応式
[Cl:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([O:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:8]([CH2:19]Cl)=[CH:7]2.[N-:21]=[N+]=[N-].[Na+]>CS(C)=O.O>[Cl:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([O:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:8]([CH2:19][NH2:21])=[CH:7]2
参加物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 57707975HCID 57707975、化合物

生成物 1

HCID 57708028HCID 57708028、化合物

試薬・触媒・溶媒 2

HCID 679Dimethyl Sulfoxide溶媒HCID 962Water溶媒

実験手順

To a solution of 8-chloro-3-(chloromethyl)-2-phenoxyquinoline (1 eq) in DMSO (0.25 M) was added NaN3 (3 eq) at rt and the mixture was stirred for 4 h at rt. The mixture was diluted with water, extracted with EtOAc (2 times) and the combined organic layers were washed with water (2 times), dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was dissolved in MeOH and treated with 10% Pd—C (5 wt %) and the mixture was then stirred under H2 balloon over night. The mixture was filtered through a Celite™ pad followed by removal of solvents to give (8-chloro-2-phenoxyquinolin-3-yl)methanamine.

後処理

  1. extractionextracted with EtOAc (2 times)
  2. washthe combined organic layers were washed with water (2 times)
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. dissolutionThe residue was dissolved in MeOH
  7. additiontreated with 10% Pd—C (5 wt %)
  8. stirringthe mixture was then stirred under H2 balloon over night
  9. filtrationThe mixture was filtered through a Celite™ pad
  10. customfollowed by removal of solvents

出典と根拠

ORDレコード
ord-61c07a89341d4c72b55d4f0ace28fa06
出典データセット
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08586739B2

反応ノート

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