반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]#[N:10].CO[CH:13]1[CH2:17][CH2:16][CH:15](OC)O1>C(O)(=O)C>[N:1]1([C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=2[CH2:8][C:9]#[N:10])[CH:13]=[CH:17][CH:16]=[CH:15]1참가 물질
4
실험 절차
Under inert atmosphere a solution of 500 mg (3.783 mmol) of 2-Aminophenylacetonitrile and 1 mL (7.566 mmol) of 2,5-Dimethoxytetrahydrofuran in 5 mL of acetic acid was heated to 60° C. for 2 hours. After cooling the reaction mixture was concentrated under reduced pressure. The residue was purified by flash chromatography on SiO2 using cyclohexane/ethyl acetate mixture of increasing polarity (from 100% cyclohexane to 100% ethyl acetate) as eluent. The title compound was obtained as a light yellow oil (470 mg, 68.2%).
후처리
- temperatureAfter cooling the reaction mixture
- concentrationwas concentrated under reduced pressure
- customThe residue was purified by flash chromatography on SiO2
- additioncyclohexane/ethyl acetate mixture
- temperatureof increasing polarity (from 100% cyclohexane to 100% ethyl acetate) as eluent
출처 및 근거
- ORD 기록
- ord-fb5b71493632416aa63df853b0a888de
- 출처 데이터셋
- uspto-grants-2014_01
- 특허 번호
- US08623901B2
연결된 노트
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