반응식
C[O:2][C:3](=O)[C:4]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[CH2:5].[NH2:13][C:14]1[N:18]=[CH:17][NH:16][N:15]=1>C(O)CCC>[C:6]1([CH:4]2[CH2:5][N:18]3[CH:17]=[N:16][N:15]=[C:14]3[NH:13][C:3]2=[O:2])[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1참가 물질
실험 절차
A solution of 9.01 g (55.6 mmol) 2-phenyl acrylic acid methyl ester and 4.24 g (50.4 mmol) 3-amino-1,2,4-triazole in 41 ml n-butanol was refluxed for 24 hours. The solvent was removed under reduced pressure. The residue was treated with a small amount of ethanol and diethyl ether and cyclohexane were added. The diethyl ether is slowly removed under reduced pressure. The crude 6-phenyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidin-7-on precipitated during evaporation, was isolated by filtration and washed with diethyl ether. 6-phenyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidin-7-on was recrystallized from a small amount of ethanol. 2.04 g (19%) 6-phenyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidin-7-on was isolated (m.p. 184-186° C.).
후처리
- customThe solvent was removed under reduced pressure
- additionThe residue was treated with a small amount of ethanol and diethyl ether and cyclohexane
- additionwere added
- customThe diethyl ether is slowly removed under reduced pressure
- customThe crude 6-phenyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidin-7-on precipitated during evaporation
- customwas isolated by filtration
- washwashed with diethyl ether
- custom6-phenyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidin-7-on was recrystallized from a small amount of ethanol
출처 및 근거
- ORD 기록
- ord-c3bbc2a121cf4b6aa6d4c1b9b88221d7
- 출처 데이터셋
- uspto-grants-2012_06
- 특허 번호
- US08192918B2
연결된 노트
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