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2-(Ethoxymethylene)propanedinitrile → 3.7-diphenyl-3H-imidazo[4,5-b]pyridine

HRID 19445
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인쇄 미리보기

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HRID 19445 반응식
[C:1]1([NH:7][C:8]2[C:13]([NH2:14])=[C:12]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[CH:11]=[CH:10][N:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:21](OC=C(C#N)C#N)C>C(O)(C)C>[C:1]1([N:7]2[C:8]3=[N:9][CH:10]=[CH:11][C:12]([C:15]4[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=4)=[C:13]3[N:14]=[CH:21]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
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참가 물질

4

반응물 2

HCID 671522-(Ethoxymethylene)propanedinitrileHCID 59346194N2,4-diphenylpyridine-2,3-diamine

생성물 1

HCID 593461673.7-diphenyl-3H-imidazo[4,5-b]pyridine수율 75%

시약·촉매·용매 1

HCID 3776Isopropanol용매

실험 절차

0.70 mol of N2,4-diphenylpyridine-2,3-diamine and 2.56 mol of ethoxymethylene malononitrile were added in 10 ml of isopropanol, and refluxed for 6 hours. The solution was removed and was purified by using column chromatography to thereby produce a solid crystalline product at a yield of 75%.

후처리

  1. temperaturerefluxed for 6 hours
  2. customThe solution was removed
  3. customwas purified
  4. customto thereby produce a solid crystalline product at a yield of 75%

출처 및 근거

ORD 기록
ord-40e8e1092dad4e8facb4458154b49562
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07745020B2

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