Diethyl (ethoxymethylene)malonate → Diethyl (6-ethoxy-2-pyridylamino)methylenemalonate

HRID 128609노트

반응식

HRID 128609 반응식
[CH2:1]([O:3][C:4]1[N:9]=[C:8]([NH2:10])[CH:7]=[CH:6][CH:5]=1)[CH3:2].C(O[CH:14]=[C:15]([C:21]([O:23][CH2:24][CH3:25])=[O:22])[C:16]([O:18][CH2:19][CH3:20])=[O:17])C>>[CH2:1]([O:3][C:4]1[N:9]=[C:8]([NH:10][CH:14]=[C:15]([C:16]([O:18][CH2:19][CH3:20])=[O:17])[C:21]([O:23][CH2:24][CH3:25])=[O:22])[CH:7]=[CH:6][CH:5]=1)[CH3:2]

참가 물질

3

반응물 2

HCID 6871Diethyl (ethoxymethylene)malonateHCID 5867106-Ethoxy-2-pyridinamine

생성물 1

HCID 86749097Diethyl (6-ethoxy-2-pyridylamino)methylenemalonate

반응 조건

온도
95 °C

실험 절차

A mixture of 6-ethoxypyridin-2-amine (8.0 g) and diethyl ethoxymethylenemalonate (12.5 g) was heated at 95° C. under vacuum for 3 hours and then heated at 95° C. at atmospheric pressure for 18 hours. The mixture was cooled to ambient temperature, diluted with petroleum ether b.p. 40°-60° C. and filtered to give diethyl (6-ethoxy-2-pyridylamino)methylenemalonate, m.p. 58°-60° C.

후처리

  1. temperatureheated at 95° C. at atmospheric pressure for 18 hours
  2. temperatureThe mixture was cooled to ambient temperature
  3. filtrationfiltered

출처 및 근거

ORD 기록
ord-6ba1fa986b1a415ca28e0a6d84dcfd3e
출처 데이터셋
uspto-grants-1995_11
특허 번호
US05464781

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