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Hydrazine → 5-Tert-butyl-1H-pyrazolo[3,4-d]pyridazin-4(5H)-one

HRID 1291222
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HRID 1291222 반응식
[C:1]([N:5]1[C:10](=[O:11])[C:9]([CH:12]=O)=[C:8]([N:14](C)C)[CH:7]=[N:6]1)([CH3:4])([CH3:3])[CH3:2].[NH2:17]N>C(O)C>[C:1]([N:5]1[C:10](=[O:11])[C:9]2[CH:12]=[N:17][NH:14][C:8]=2[CH:7]=[N:6]1)([CH3:4])([CH3:3])[CH3:2]
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참가 물질

4

반응물 2

HCID 9321HydrazineHCID 189188952-Tert-butyl-5-dimethylamino-4-formyl-3(2H)-pyridazinone

생성물 1

HCID 189191095-Tert-butyl-1H-pyrazolo[3,4-d]pyridazin-4(5H)-one

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

2-Tert-butyl-5-dimethylamino-4-formyl-3(2H)-pyridazinone (3.5 g) was added to hydrazine (5.1 g)/ethanol (30 ml) and the mixture was refluxed for 40 hours. The solvent ethanol-hydrazine was then distilled off and the residue was extracted with ethyl acetate. The organic layer was washed with saturated aqueous NaCl solution, dried over anhydrous magnesium sulfate, and concentrated to dryness. The residue was washed with n-hexane-diethyl ether and dried. White powder, 1.9 g. 1H-NMR (CDCl3) δ: 1.71(9H,s), 8.19(1H,s), 8.32(1H,s).

후처리

  1. temperaturethe mixture was refluxed for 40 hours
  2. distillationThe solvent ethanol-hydrazine was then distilled off
  3. extractionthe residue was extracted with ethyl acetate
  4. washThe organic layer was washed with saturated aqueous NaCl solution
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated to dryness
  7. washThe residue was washed with n-hexane-diethyl ether
  8. customdried

출처 및 근거

ORD 기록
ord-585dbe4cf4c84746b9db287b5f2cf064
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05753664

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