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Hydrazine hydrate (1:1) → 6,7-Dihydropyrido[2,3-d]pyridazine-5,8-dione

HRID 1166061
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HRID 1166061 반응식
O.[NH2:2][NH2:3].[N:4]1[CH:9]=[CH:8][CH:7]=[C:6]2[C:10](O[C:13](=[O:14])[C:5]=12)=[O:11].C([O-])(=O)C.[Na+]>C(O)(=O)C.O>[N:4]1[C:5]2[C:13](=[O:14])[NH:2][NH:3][C:10](=[O:11])[C:6]=2[CH:7]=[CH:8][CH:9]=1
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참가 물질

5

반응물 3

HCID 24654Hydrazine hydrate (1:1)HCID 69688Furo[3,4-b]pyridine-5,7-dioneHCID 517045Sodium Acetate

생성물 1

HCID 2207116,7-Dihydropyrido[2,3-d]pyridazine-5,8-dione수율 76.2%

시약·촉매·용매 1

HCID 21899381Acetic acid--water (1/1)용매

실험 절차

Hydrazine hydrate (13.09 g, 0.261 mol) was added to a stirred solution of pyridine-2,3-dicarboxylic anhydride (30.0 g, 0.201 mol) and sodium acetate (21.45 g, 0.261 mol) in 40% acetic acid/water (400 ml). The reaction was heated at reflux for 3 days under nitrogen. The yellow precipitate was filtered off and washed successively with water (4×200 ml), hexane (3×150 ml) and diethyl ether (3×150 ml) to give the title-compound (25.0 g, 76%), 1H NMR (250 MHz, d6-DMSO) δ 7.90 (1H, q, J=4.5Hz, Ar—H), 8.51 (1H, d, J=4.5Hz, Ar—H), 9.13 (1H, d, J=4.6Hz, Ar—H), 11.65 (2H, br s, 2 of NH); MS (ES+) m/e 164 [MH]+.

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후처리

  1. temperatureThe reaction was heated
  2. temperatureat reflux for 3 days under nitrogen
  3. filtrationThe yellow precipitate was filtered off
  4. washwashed successively with water (4×200 ml), hexane (3×150 ml) and diethyl ether (3×150 ml)

출처 및 근거

ORD 기록
ord-4090e406b46f422aa0e5063089bcee0a
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06613766B1

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