반응식
C(=O)([O-])[O-].[K+].[K+].[Cl:7]C1C=C(N2CCN(C[CH2:21][CH2:22][N:23]3[C:27](=[O:28])[N:26]=[C:25](CC)[NH:24]3)CC2)C=CC=1.[O:31](CCBr)[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1.[I-].[K+].ClC1C=C(N2CCN(CCCN3C(=O)N(CCOC4C=CC=CC=4)C(CC)=N3)CC2)C=CC=1.Cl>C(#N)C.C(O)C>[ClH:7].[O:31]([CH2:21][CH2:22][N:23]1[C:27](=[O:28])[NH:26][CH:25]=[N:24]1)[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1참가 물질
실험 절차
Reaction in Acetonitrile With Potassium Carbonate. A mixture of 2-[3-[4-(3-chlorophenyl)-1-piperazinyl]propyl]-5-ethyl-1H-1,2,4-triazol-3(2H)-one (15 g., 0.043 mole), phenoxyethyl bromide (8.62 g., 0.043 mole), potassium carbonate (11.9 g., 0.086 mole) and a trace of potassium iodide in 100 ml. of acetonitrile is refluxed for a 64 hr. period. The reaction mixture is filtered, the filtrate concentrated under reduced pressure and residual material taken up in ether and filtered. Concentration of the ethereal filtrate affords 18.35 g. (91%) of the free base product 2-[3-[4-(3-chlorophenyl)-1-piperazinyl]propyl]-5-ethyl-4-(2-phenoxyethyl)-2H-1,2,4-triazol-3(4H)-one. The free base is converted to the hydrochloride in ethanol employing ethanolic hydrogenchloride and crystallized from ethanol to afford a 53% yield of analytically pure 2-[3-[4-(3-chlorophenyl)-1-piperazinyl]propyl]-5 -ethyl-4-(2-phenoxyethyl-2H-1,2,4-triazol-3(4H)-one hydrochloride, m.p. 175°-177° C.
후처리
- filtrationThe reaction mixture is filtered
- concentrationthe filtrate concentrated under reduced pressure and residual material
- filtrationfiltered
- customConcentration of the ethereal filtrate affords 18.35 g
- customcrystallized from ethanol
출처 및 근거
- ORD 기록
- ord-36ffb88d24914d9d91689d9ec5358028
- 출처 데이터셋
- uspto-grants-1986_03
- 특허 번호
- US04575555
연결된 노트
불러오는 중…