(Phenylmethyl)hydrazine → 3,4-Dichloro-6-phenylpyridazine

HRID 227821

반응식

HRID 227821 반응식
[O:1]=[C:2](CCC1C=CC=CC=1)C(O)=O.C1(CNN)C=CC=CC=1.[Cl:23][C:24]1[N:25]=[N:26][C:27]([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)=[CH:28][C:29]=1[Cl:30].[CH3:37][O-:38].[Na+]>CO>[Cl:23][C:24]1[N:25]=[N:26][C:27]([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)=[CH:28][C:29]=1[Cl:30].[CH3:2][O:1][C:24]1[N:25]=[N:26][C:27]([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)=[CH:28][C:29]=1[O:38][CH3:37].[CH3:2][O:1][C:24]1[N:25]=[N:26][C:27]([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)=[CH:28][C:29]=1[Cl:30]

참가 물질

8

반응물 4

HCID 11157(Phenylmethyl)hydrazineHCID 697322-Oxo-4-phenylbutyric acidHCID 10942334Sodium MethoxideHCID 131632313,4-Dichloro-6-phenylpyridazine

생성물 3

HCID 131632313,4-Dichloro-6-phenylpyridazineHCID 13342056HCID 13342056, 화합물HCID 66731998HCID 66731998, 화합물

시약·촉매·용매 1

HCID 887Methanol용매2회

반응 조건

온도
65 °C

실험 절차

3,4-Dichloro-6-phenylpyridazine was synthesized from □-oxobenzenebutanoic acid and 1-(phenylmethyl)hydrazine in 2 steps according to a procedure by Sircar (Sircar, I. J Het. Chem. 1983, 20,1473-1476.) 3,4-Dichloro-6-phenylpyridazine (100 mg, 0.44 mmol) was combined with sodium methoxide (1.1 mL of a 0.50M solution in methanol, 0.55 mmol, 1.25 equiv.) and methanol (296 μl, 1.5M) in a resealable tube and heated to 65° C. for 1 hour. The methanol was evaporated in vacuo, and water was added to the residue. The mixture was extracted with DCM, dried over K2CO3, filtered and concentrated in vacuo, to afford 3,4-dimethoxy-6-phenylpyridazine and 3-methoxy-4-chloro-6-phenylpyridazine, the title compound, as a solid.

후처리

  1. customThe methanol was evaporated in vacuo, and water
  2. additionwas added to the residue
  3. extractionThe mixture was extracted with DCM
  4. dry with materialdried over K2CO3
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-667bead50e7a433e8d7e7c138df62023
출처 데이터셋
uspto-grants-2009_07
특허 번호
US07560551B2

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