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(4-Amino-3-nitrophenyl)-2-pyridinylmethanone → HCID 21432586, 화합물

HRID 2399034
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HRID 2399034 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([CH:15]=[CH:16][C:17]=1[NH2:18])[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=1)=[O:8])([O-])=O.[H][H]>O1CCCC1.[Pd]>[NH2:1][C:4]1[CH:5]=[C:6]([CH:15]=[CH:16][C:17]=1[NH2:18])[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=1)=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 21432596(4-Amino-3-nitrophenyl)-2-pyridinylmethanoneHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 21432586HCID 21432586, 화합물

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8028Tetrahydrofuran용매

실험 절차

A suspension of 20 g. (0.082 mol) of 2-(3-nitro-4-aminobenzoyl)pyridine in 1 liter of tetrahydrofuran containing 5 g. of 5% palladium on carbon was reduced with hydrogen under a pressure of 3 atmospheres. The resulting mixture was filtered and concentrated in vacuo to a reddish oil which was dissolved in a minimum amount of methylene chloride and diluted with petroleum ether to yield 2-(3,4-diaminobenzoyl)pyridine as a slightly unstable yellow solid, mp. 137° -138° C. (water).

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후처리

  1. additionA suspension of 20 g
  2. filtrationThe resulting mixture was filtered
  3. concentrationconcentrated in vacuo to a reddish oil which
  4. dissolutionwas dissolved in a minimum amount of methylene chloride
  5. additiondiluted with petroleum ether

출처 및 근거

ORD 기록
ord-a4de091a8de5459dab2de92f4a1824c8
출처 데이터셋
uspto-grants-1977_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04026936

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