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HRID 484512作成日:2026年10月25日

Sodium Carbonate → 3-Bromo-6-[4-[3-[4-(4,5-dihydro-2-oxazolyl)phenoxy]propyl]-1-piperazinyl]pyridazine

https://huagongshe.com/reaction/484512

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物3,6-DibromopyridazineHCID 248852—
反応物1-[3-[4-(4,5-Dihydro-2-oxazolyl)phenoxy]propyl]piperazineHCID 14989179—
溶媒DimethylformamideHCID 6228—
生成物3-Bromo-6-[4-[3-[4-(4,5-dihydro-2-oxazolyl)phenoxy]propyl]-1-piperazinyl]pyridazineHCID 1498929716.4%

反応条件

温度65 °C

反応手順

A mixture of 4.1 parts of 3,6-dibromopyridazine, 4.34 parts of 1-[3-[4-(4,5-dihydro-2-oxazolyl)phenoxy]propyl]piperazine, 6.4 parts of sodium carbonate and 1878 parts of N,N-dimethylformamide was stirred overnight at 65° C. The reaction mixture was poured into ice water and the product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol 98.5:1.5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2-propanol. The product was filtered off and dried, yielding 1.1 parts (16.4%) of 3-bromo-6-[4-[3-[4(4,5-dihydro-2-oxazolyl)phenoxy]propyl]-1-piperazinyl]pyridazine; mp. 169.1° C. (comp. 75).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05231184
出典データセットuspto-grants-1993_07
ORD IDord-88af42f5eb6e40948beb22d5d10e5c98
出典メモuspto-grants-1993_07