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Water → 2,4-Dimethylpyridin-3-amine

HRID 1811584
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HRID 1811584 반응식
[CH3:1][C:2]1[N:10]=[CH:9][CH:8]=[C:7]([CH3:11])[C:3]=1C(O)=O.[N-:12]=[N+]=[N-].[Na+].O>O=S(Cl)Cl>[CH3:1][C:2]1[C:3]([NH2:12])=[C:7]([CH3:11])[CH:8]=[CH:9][N:10]=1
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참가 물질

5

반응물 3

HCID 962WaterHCID 33557Sodium AzideHCID 15125612,4-Dimethyl-3-pyridinecarboxylic acid

생성물 1

HCID 149107812,4-Dimethylpyridin-3-amine

시약·촉매·용매 1

HCID 24386Thionyl Chloride용매

반응 조건

온도
60 °C

실험 절차

2,4-dimethylnicotinic acid (3.0 g, 20 mmol) was added in SOCl2 (20 mL) at 0° C. and warmed to 60° C. After stirring for 1 hr, the reaction was concentrated under vacuum. The residue was dissolved in acetone (20 mL) and NaN3 (1.9 g, 30 mmol) followed by H2O (20 mL). The reaction was warmed to 70° C. and stirred for 1 hr at the same temperature. The reaction was cooled to room temperature and concentrated under vacuum to a half volume and poured into H2O (50 mL) and extracted with ethyl acetate (50 mL×5) and dried over MgSO4. The ethyl acetate was concentrated under vacuum to afford the crude compound. The compound was used for the next step without further purification. 1HNMR (CDCl3, 400 MHz) δ 2.10 (s, 3H), 2.30 (s, 3H), 4.65-4.70 (b, 2H), 6.85 (d, J=4.78 Hz, 1H), 7.75 (d, J=4.78 Hz, 1H). Exact mass calculated for C7H10N2 122.08. found 123.1 (MH+).

후처리

  1. concentrationthe reaction was concentrated under vacuum
  2. dissolutionThe residue was dissolved in acetone (20 mL)
  3. temperatureThe reaction was warmed to 70° C.
  4. stirringstirred for 1 hr at the same temperature
  5. temperatureThe reaction was cooled to room temperature
  6. concentrationconcentrated under vacuum to a half volume
  7. additionpoured into H2O (50 mL)
  8. extractionextracted with ethyl acetate (50 mL×5)
  9. dry with materialdried over MgSO4
  10. concentrationThe ethyl acetate was concentrated under vacuum

출처 및 근거

ORD 기록
ord-9ea332d0f2e04c0bb4a1035eae1ee46b
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08362248B2

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