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

HRID 1534940
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HRID 1534940 반응식
[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
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참가 물질

4

반응물 2

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

생성물 1

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

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

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%.

후처리

  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

출처 및 근거

ORD 기록
ord-9d23d13dfa55404ab0a539089fa710a0
출처 데이터셋
uspto-grants-1992_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05091432

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