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Formic Acid → 6-Amino-4-methylnicotinaldehyde

HRID 534778
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HRID 534778 반응식
[C:1]([C:3]1[C:4]([CH3:16])=[CH:5][C:6]([NH:9]C(=O)C(F)(F)F)=[N:7][CH:8]=1)#N.C(O)=[O:18]>O.[Ni].[Al]>[NH2:9][C:6]1[N:7]=[CH:8][C:3]([CH:1]=[O:18])=[C:4]([CH3:16])[CH:5]=1
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참가 물질

5

반응물 2

HCID 284Formic AcidHCID 86618113N-(5-Cyano-4-methyl-2-pyridinyl)-2,2,2-trifluoroacetamide

생성물 1

HCID 552846706-Amino-4-methylnicotinaldehyde

시약·촉매·용매 2

HCID 962Water용매HCID 6336846Nickel aluminide용매

실험 절차

A solution of N-(5-cyano-4-methyl-2-pyridinyl)-2,2,2-trifluoroacetamide (D98) (0.050 g, 0.22 mmol) in formic acid (1.35 mL) was diluted with water (0.48 mL) and nickel/aluminium alloy (0.122 g) was added. The reaction mixture was heated at reflux under argon for 2 h then filtered while still hot, washing with further formic acid (3×5 mL). The filtrate and washings were concentrated, diluted with toluene (5 mL) and re-concentrated to give the crude title compound as a pale yellow solid (0.053 g) which was used in the next step without further purification. δH (CDCl3, 400 MHz) 9.91 (1H, s), 8.34 (1H, s), 6.31 (1H, s), 5.49 (2H, br.s), 2.57 (3H, s). MS (ES): MH+ 137.2.

후처리

  1. additionwas added
  2. temperatureThe reaction mixture was heated
  3. temperatureat reflux under argon for 2 h
  4. filtrationthen filtered while still hot,
  5. washwashing with further formic acid (3×5 mL)
  6. concentrationThe filtrate and washings were concentrated
  7. additiondiluted with toluene (5 mL)
  8. concentrationre-concentrated

출처 및 근거

ORD 기록
ord-9e428a7ab77b46909408c508c5735e81
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08853218B2

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