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Acetic Acid → 3-Amino-7-chloro-2-methylimidazo[2,1-a]isoquinoline

HRID 649156
ノート
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反応式

HRID 649156 の反応式
[Cl:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][N:6]1[C:14]([N:15]=O)=[C:13]([CH3:17])[N:12]=[C:7]12.C(O)(=O)C>O.[Zn]>[NH2:15][C:14]1[N:6]2[CH:5]=[CH:4][C:3]3[C:8]([C:7]2=[N:12][C:13]=1[CH3:17])=[CH:9][CH:10]=[CH:11][C:2]=3[Cl:1]
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 176Acetic AcidHCID 138218497-Chloro-2-methyl-3-nitrosoimidazo[2,1-a]isoquinoline

生成物 1

HCID 201424413-Amino-7-chloro-2-methylimidazo[2,1-a]isoquinoline収率 80.6%

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 962Water溶媒

実験手順

Zinc powder (10.2 g) was added portionwise to a mixture of 7-chloro-2-methyl-3-nitrosoimidazo[2,1-a]isoquinoline (7.7 g) and acetic acid (100 ml) in water (77 ml) over a period of 7 hours and then the mixture was filtered by suction. The filtrate was evaporated in vacuo and the residue was extracted with chloroform after an addition of aqueous sodium bicarbonte to it. The extract was washed with water and evaporated in vacuo. The residual solid was washed with ethyl acetate and dried in a desiccator to give 3-amino-7-chloro-2-methylimidazo[2,1-a]isoquinoline (5.85 g).

後処理

  1. filtrationthe mixture was filtered by suction
  2. customThe filtrate was evaporated in vacuo
  3. extractionthe residue was extracted with chloroform
  4. additionafter an addition of aqueous sodium bicarbonte to it
  5. washThe extract was washed with water
  6. customevaporated in vacuo
  7. washThe residual solid was washed with ethyl acetate
  8. customdried in a desiccator

出典と根拠

ORDレコード
ord-d6b7d2cda5e544c38c0a052e91cb32fd
出典データセット
uspto-grants-1988_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04738967

反応ノート

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