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Hydrazine hydrate (1:1) → 3-(6-Oxo-3,6-dihydro-9H-purin-9-yl)propanehydrazide

HRID 1534940
ノート
印刷プレビュー

反応式

HRID 1534940 の反応式
[O:1]=[C:2]1[NH:10][CH:9]=[N:8][C:7]2[N:6]([CH2:11][CH2:12][C:13]([O:15]CC)=O)[CH:5]=[N:4][C:3]1=2.O.[NH2:19][NH2:20]>C(O)C>[O:1]=[C:2]1[NH:10][CH:9]=[N:8][C:7]2[N:6]([CH2:11][CH2:12][C:13]([NH:19][NH2:20])=[O:15])[CH:5]=[N:4][C:3]1=2
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24654Hydrazine hydrate (1:1)HCID 135794781Ethyl 3-(6-oxo-3,6-dihydro-9H-purin-9-yl)propanoate

生成物 1

HCID 1362413973-(6-Oxo-3,6-dihydro-9H-purin-9-yl)propanehydrazide収率 80.1%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

1.181 g (5.00 mmol) of 3-(1,6-dihydro-6-oxo-9H-purin-9-yl)propionic acid, ethyl ester (AIT-0027) was placed into a 25 ml flask equipped with a magnetic stirring bar. About 5 ml absolute ethanol was added and then 2.50 g (50.00 mmol) of hydrazine hydrate was added and the solution was stirred at room temperature in a closed flask. A large amount of precipitate formed after about 30 minutes and the solution was allowed to stand overnight. The solution was filtered by vacuum and the white solid was washed with ethanol and then with ether. Upon drying, 0.890 g of 3-(1,6-dihydro-6-oxo-9H-purin-9-yl)propanoic acid hydrazide (AIT-0056) as a white solid was obtained. Yield: 80%.

後処理

  1. customequipped with a magnetic stirring bar
  2. customA large amount of precipitate formed after about 30 minutes
  3. filtrationThe solution was filtered by vacuum
  4. washthe white solid was washed with ethanol
  5. customUpon drying

出典と根拠

ORDレコード
ord-9d23d13dfa55404ab0a539089fa710a0
出典データセット
uspto-grants-1992_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05091432

反応ノート

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