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[OH:1][CH2:2][CH2:3][NH:4][N:5]=[CH:6][C:7](=[N:10][OH:11])[C:8]#[N:9]>C(O)CCC>[NH2:9][C:8]1[N:4]([CH2:3][CH2:2][OH:1])[N:5]=[CH:6][C:7]=1[N:10]=[O:11]참가 물질
3
실험 절차
In a flask having an inner volume of 25 ml and equipped with a stirring device, a thermometer and a reflux condenser were charged 0.94 g (6 mmol) of 3-(2-hydroxyethyl)hydrazono-2-hydroxyiminopropionitrile synthesized by the same method as in Example 5 and 6 ml of n-butyl alcohol, and the mixture was reacted at 110° C. for 3 hours, and further at 5 to 10° C. for 1 hour. After completion of the reaction, the reaction mixture was filtered, and the filtrate was dried under reduced pressure to give 0.61 g (isolation yield: 64%) of 5-amino-1-(2-hydroxyethyl)-4-nitrosopyrazole as reddish orange crystal.
후처리
- customIn a flask having
- customan inner volume of 25 ml and equipped with a stirring device
- customthe mixture was reacted at 110° C. for 3 hours
- customAfter completion of the reaction
- filtrationthe reaction mixture was filtered
- customthe filtrate was dried under reduced pressure
출처 및 근거
- ORD 기록
- ord-d98a8146174f46c5bc979274264d70b0
- 출처 데이터셋
- uspto-grants-2007_08
- 특허 번호
- US07256304B2
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