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Pyrazole, 3-amino-4-cyano-5-ethyl- → 2-Ethyl-7-(3-pyridyl)pyrazolo[1,5-a]pyrimidine-3-carbonitrile

HRID 1278198
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인쇄 미리보기

반응식

HRID 1278198 반응식
[NH2:1][C:2]1[C:6]([C:7]#[N:8])=[C:5]([CH2:9][CH3:10])[NH:4][N:3]=1.CN(C)[CH:13]=[CH:14][C:15]([C:17]1[CH:18]=[N:19][CH:20]=[CH:21][CH:22]=1)=O>C(O)(=O)C>[CH2:9]([C:5]1[C:6]([C:7]#[N:8])=[C:2]2[N:1]=[CH:13][CH:14]=[C:15]([C:17]3[CH:18]=[N:19][CH:20]=[CH:21][CH:22]=3)[N:3]2[N:4]=1)[CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 114021Pyrazole, 3-amino-4-cyano-5-ethyl-HCID 5670331-(3-Pyridyl)-3-(dimethylamino)-2-propen-1-one

생성물 1

HCID 113456772-Ethyl-7-(3-pyridyl)pyrazolo[1,5-a]pyrimidine-3-carbonitrile

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

As for Example 2, 2.72 g. of 3-amino-5-ethylpyrazole-4-carbonitrile is heated at reflux temperature for 16 hours with 3.52 g. of 3-dimethylamino-1-(3-pyridyl)-2-propen-1-one in 25 ml. of glacial acetic acid to give 2.65 g. of the product of the example as colorless crystals, m.p. 170°-172° C.

후처리

  1. temperatureat reflux temperature for 16 hours with 3.52 g

출처 및 근거

ORD 기록
ord-7717df1e1ad04ec592ca9a30f3d9a2e4
출처 데이터셋
uspto-grants-1981_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04281000

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