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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Dimethylformamide dimethyl acetal → 6-(2-(Dimethylamino)vinyl)-2-ethoxy-5-nitronicotinonitrile

HRID 2407836
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인쇄 미리보기

반응식

HRID 2407836 반응식
[CH2:1]([O:3][C:4]1[N:11]=[C:10]([CH3:12])[C:9]([N+:13]([O-:15])=[O:14])=[CH:8][C:5]=1[C:6]#[N:7])[CH3:2].CO[CH:18](OC)[N:19]([CH3:21])[CH3:20]>CN(C)C=O>[CH3:18][N:19]([CH3:21])[CH:20]=[CH:12][C:10]1[C:9]([N+:13]([O-:15])=[O:14])=[CH:8][C:5]([C:6]#[N:7])=[C:4]([O:3][CH2:1][CH3:2])[N:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 78373Dimethylformamide dimethyl acetalHCID 585042232-Ethoxy-6-methyl-5-nitronicotinonitrile

생성물 1

HCID 768067286-(2-(Dimethylamino)vinyl)-2-ethoxy-5-nitronicotinonitrile

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a stirred solution of the compound prepared in Example 444 (0.86 g) in N,N-dimethylformamide (10 mL) at ambient temperature was added N,N-dimethylformamide dimethyl acetal (94%, 0.65 mL). The resulting solution was stirred and heated to reflux for 30 minutes. After cooling to ambient temperature, the solution was concentrated to provide the title compound (1.07 g) with the following physical data.

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후처리

  1. temperatureheated
  2. temperatureto reflux for 30 minutes
  3. concentrationthe solution was concentrated

출처 및 근거

ORD 기록
ord-969f582f9c30443994fbc2d2ecf658ba
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08809538B2

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