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N'-(7-Chloro-6-(4-methoxyphenyl)-pyrido[2,3-d]pyrimidin-2-yl)-N,N-dimethyl-formamidine → 2-Amino-7-chloro-6-(4-methoxyphenyl)-pyrido[2,3-d]-pyrimidine

HRID 3413
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인쇄 미리보기

반응식

HRID 3413 반응식
[Cl:1][C:2]1[C:3]([C:17]2[CH:22]=[CH:21][C:20]([O:23][CH3:24])=[CH:19][CH:18]=2)=[CH:4][C:5]2[CH:10]=[N:9][C:8]([N:11]=CN(C)C)=[N:7][C:6]=2[N:16]=1>C(O)C>[NH2:11][C:8]1[N:9]=[CH:10][C:5]2[CH:4]=[C:3]([C:17]3[CH:18]=[CH:19][C:20]([O:23][CH3:24])=[CH:21][CH:22]=3)[C:2]([Cl:1])=[N:16][C:6]=2[N:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 53718994N'-(7-Chloro-6-(4-methoxyphenyl)-pyrido[2,3-d]pyrimidin-2-yl)-N,N-dimethyl-formamidine

생성물 1

HCID 218500162-Amino-7-chloro-6-(4-methoxyphenyl)-pyrido[2,3-d]-pyrimidine수율 32.2%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 10 g of N'-(7-chloro-6-(4-methoxy-phenyl)-pyrido[2,3-d]pyrimidin-2-yl)-N,N-dimethyl-formamidine from Example 11 and 500 mL of 95% ethanol was refluxed for 3 hours. The solution was concentrated in vacuo and the precipitate collected by filtration. Crystallization from ethanol afforded 2.7 g of the title compound 2-amino-7-chloro-6-(4-methoxyphenyl)-pyrido[2,3-d]pyrimidine, mp 275°-280° C. dec.

후처리

  • temperaturewas refluxed for 3 hours
  • concentrationThe solution was concentrated in vacuo
  • filtrationthe precipitate collected by filtration
  • customCrystallization from ethanol
  • 출처 및 근거

    ORD 기록
    ord-86096de2e5674031bab10b49fa871e15
    출처 데이터셋
    uspto-grants-1998_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05733913

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