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Diethyl (ethoxymethylene)malonate → HCID 18000191, 화합물

HRID 2184748
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HRID 2184748 반응식
[CH2:1]([NH:8][C:9]1[CH:14]=[CH:13][C:12]([NH2:15])=[CH:11][N:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(O[CH:19]=[C:20]([C:26]([O:28][CH2:29][CH3:30])=[O:27])[C:21]([O:23][CH2:24][CH3:25])=[O:22])C>>[CH2:1]([NH:8][C:9]1[CH:14]=[CH:13][C:12]([NH:15][CH:19]=[C:20]([C:21]([O:23][CH2:24][CH3:25])=[O:22])[C:26]([O:28][CH2:29][CH3:30])=[O:27])=[CH:11][N:10]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 6871Diethyl (ethoxymethylene)malonateHCID 3629459HCID 3629459, 화합물

생성물 1

HCID 18000191HCID 18000191, 화합물수율 84.1%

반응 조건

온도
130 °C

실험 절차

A mixture of 2-benzylamino-5-aminopyridine (1.76 g) and diethyl ethoxymethylenemalonate (1.78 mL, 8.82 mmol) was heated at 130° C. for 2 h. While warm, the mixture was evacuated. After cooling, the product was triturated with 2:1 hexanes/ether and collected to give 2.74 g of diethyl (2-benzylamino-5-pyridylaminomethylene)malonate as a gold solid.

후처리

  1. temperatureWhile warm
  2. customthe mixture was evacuated
  3. temperatureAfter cooling
  • customthe product was triturated with 2:1 hexanes/ether
  • customcollected
  • 출처 및 근거

    ORD 기록
    ord-563f22efed754fbeba49cf05815423d3
    출처 데이터셋
    uspto-grants-2002_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06399604B1

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