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Dimethylformamide dimethyl acetal → HCID 178430874, 화합물

HRID 2297172
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HRID 2297172 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9](=[O:17])[CH2:10][C:11]1[NH:12][CH:13]=[C:14]([CH3:16])[N:15]=1.CO[CH:20](OC)[N:21]([CH3:23])[CH3:22]>>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9](=[O:17])/[C:10](/[C:11]1[NH:12][CH:13]=[C:14]([CH3:16])[N:15]=1)=[CH:20]\[N:21]([CH3:23])[CH3:22]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 78373Dimethylformamide dimethyl acetalHCID 1784308761-(2,4-Dichlorophenyl)-2-(4-methylimidazol-2-yl)ethan-1-one

생성물 1

HCID 178430874HCID 178430874, 화합물

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온도
72.5 °C

실험 절차

A mixture of 1-(2,4-dichlorophenyl)-2-(4-methylimidazol-2-yl)ethan-1-one (0.33 M) and N,N-dimethylformamide-dimethyl acetal (DMFDMA) (25 ml) was stirred for 2.5 h at 70-75° C. The DMFDMA was then removed under reduced pressure and dried under high vacuum for several hours giving a light orange solid in quantitative yield. The enaminone product (2Z)-1-(2,4-dichlorophenyl)-3-(dimethylamino)-2-(4-methylimidazol-2-yl)prop-2-en-1-one was typically used without further purification.

후처리

  1. custom
The DMFDMA was then removed under reduced pressure
  • customdried under high vacuum for several hours
  • customgiving a light orange solid in quantitative yield
  • customThe enaminone product (2Z)-1-(2,4-dichlorophenyl)-3-(dimethylamino)-2-(4-methylimidazol-2-yl)prop-2-en-1-one was typically used without further purification
  • 출처 및 근거

    ORD 기록
    ord-73c08f49afbb4d0eb279daed6d02d525
    출처 데이터셋
    uspto-grants-2002_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06489344B1

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