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Methyl 5-(4-methoxy-3-nitrophenyl)-3-pyridinecarboxylate → HCID 19837271, 화합물

HRID 477048
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인쇄 미리보기

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HRID 477048 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:10]=[N:11][CH:12]=[C:13]([CH:18]=2)[C:14]([O:16][CH3:17])=[O:15])=[CH:5][C:4]=1[N+:19]([O-])=O>C(OCC)(=O)C.[C].[Pd]>[NH2:19][C:4]1[CH:5]=[C:6]([C:9]2[CH:10]=[N:11][CH:12]=[C:13]([CH:18]=2)[C:14]([O:16][CH3:17])=[O:15])[CH:7]=[CH:8][C:3]=1[O:2][CH3:1]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 14769996Methyl 5-(4-methoxy-3-nitrophenyl)-3-pyridinecarboxylate2회

생성물 1

HCID 19837271HCID 19837271, 화합물수율 81.5%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 8857Ethyl Acetate용매

반응 조건

온도
50 °C

실험 절차

990 mg of the resulting nitro compound was dissolved in 60 ml of ethyl acetate, and 0.3 g of 10% palladium-carbon was added. The nitro compounds was thus catalytically reduced with stirring at 50° C. The catalyst was removed in a customary manner, and the resulting yellow crystals were recrystallized from methylene chloride-ether to give 723 mg (yield 81%) of methyl 5-(3-amino-4-methoxyphenyl)nicotinate as pale yellow needles having a melting point of 98° to 99° C.

후처리

  1. customThe catalyst was removed in a customary manner
  2. customthe resulting yellow crystals were recrystallized from methylene chloride-ether

출처 및 근거

ORD 기록
ord-82c4dd22dec043b6ac03a755302ac152
출처 데이터셋
uspto-grants-1989_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04886822

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