Ethyl cyanoacetate → 6-Amino-2-(2-propoxyphenyl)pyrimidin-4[3H]-one
반응식
[C:1]([CH2:3][C:4](OCC)=[O:5])#[N:2].[CH2:9]([O:12][C:13]1[CH:21]=[CH:20][CH:19]=[CH:18][C:14]=1[C:15]([NH2:17])=[NH:16])[CH2:10][CH3:11]>C(O)C.O>[NH2:2][C:1]1[N:17]=[C:15]([C:14]2[CH:18]=[CH:19][CH:20]=[CH:21][C:13]=2[O:12][CH2:9][CH2:10][CH3:11])[NH:16][C:4](=[O:5])[CH:3]=1참가 물질
실험 절차
Ethyl cyanoacetate (4.52 g) was added to a stirred solution of 2-propoxybenzamidine in ethanol (prepared from sodium, 1.84 g., in ethanol, 100 ml, and 2-propoxybenzamidine methanesulphonate, 11.61 g). The reaction mixture was stirred at ambient temperature for 18 hours and then evaporated under reduced pressure to leave a residue which was dissolved in water. The aqueous solution was extracted with diethyl ether (2×25 ml) and the combined ether extracts were washed with water. The combined aqueous phase was treated with glacial acetic acid to pH 5 to precipitate a crude product. Further crude product was obtained by extracting the ether extracts with 1 normal sodium hydroxide (2×30 ml) and acidifying the combined alkaline extracts with glacial acetic acid to pH 5. The combined crude product was recrystallised from isopropanol to yield the title compound, 2.34 g, m.p. 183.5°-184.5° C.
후처리
- customevaporated under reduced pressure
- customto leave a residue which
- extractionThe aqueous solution was extracted with diethyl ether (2×25 ml)
- washthe combined ether extracts were washed with water
- additionThe combined aqueous phase was treated with glacial acetic acid to pH 5
- customto precipitate a crude product
- customFurther crude product was obtained
- extractionby extracting the ether
- customwas recrystallised from isopropanol
출처 및 근거
- ORD 기록
- ord-660ba3151f6b40d89065c2d132e6651e
- 출처 데이터셋
- uspto-grants-1992_06
- 특허 번호
- US05118686
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