반응식
Cl.[NH2:2][C:3]1[N:7]([CH2:8][CH2:9][OH:10])[N:6]=[CH:5][C:4]=1[N:11]=[O:12].O.N>C(O)(C)C>[NH2:2][C:3]1[N:7]([CH2:8][CH2:9][OH:10])[N:6]=[CH:5][C:4]=1[N:11]=[O:12]참가 물질
반응 조건
- 온도
- 5 °C
실험 절차
To a flask having an inner volume of 25 ml and equipped with a stirring device and a thermometer were charged 2.10 g (10 mmol) of 5-amino-1-(2-hydroxyethyl)-4-nitrosopyrazole hydrochloride with a purity of 91.6% by weight synthesized in the same manner as in Example 4, 3.5 ml of water and 0.5 ml of isopropyl alcohol. Then, 1 ml (16 mmol) of 28% aqueous ammonia was gradually added dropwise to the mixture, and the resulting mixture was reacted for 30 minutes while maintaining the liquid temperature to 5° C. or lower. After completion of the reaction, precipitated crystals were collected by filtration. Then, the crystals were washed with 1 ml of cold water and 1 ml of cold isopropyl alcohol, and then dried at 40° C. under reduced pressure to obtain 1.13 g of 5-amino-1-(2-hydroxyethyl)-4-nitrosopyrazole (Isolation yield: 72.0%) as reddish orange crystal with a purity of 99.7% by weight (absolute calibration curve method by high performance liquid chromatography).
후처리
- customTo a flask having
- customan inner volume of 25 ml and equipped with a stirring device
- customthe resulting mixture was reacted for 30 minutes
- customAfter completion of the reaction
- customprecipitated crystals
- filtrationwere collected by filtration
- washThen, the crystals were washed with 1 ml of cold water and 1 ml of cold isopropyl alcohol
- customdried at 40° C. under reduced pressure
출처 및 근거
- ORD 기록
- ord-881c035807794269a7218507ec340c97
- 출처 데이터셋
- uspto-grants-2007_06
- 특허 번호
- US07227032B2
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