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HRID 486509作成日:2026年10月26日

5,5-dimethyl-1-pyrroline N-oxide → (Cis)-2-butyl-6-(hexahydro-6,6-dimethylpyrrolo[1,2-b]isoxazol-2-yl)-3-[[2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-4(3H)-quinazolinone

https://huagongshe.com/reaction/486509

反応式

関与物質

役割名称HCID仕込み量
反応物5,5-dimethyl-1-pyrroline N-oxideHCID 1774—
反応物2-Butyl-6-ethenyl-3-[[2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-4(3H)-quinazolinoneHCID 15233931—
溶媒TolueneHCID 1140—
生成物(Cis)-2-butyl-6-(hexahydro-6,6-dimethylpyrrolo[1,2-b]isoxazol-2-yl)-3-[[2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl]methyl]-4(3H)-quinazolinoneHCID 5731714757.2%

反応手順

To a solution of 0.500 g of 2-Butyl-6-ethenyl-3-[[2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl]-[1,1'-biphenyl]-4-yl]methyl]-4(3H)-quinazolinone in 25 ml of toluene is added 0.161 g of 5,5-dimethyl-1-pyrroline N-oxide and the reaction mixture heated at reflux for 6 hours. The reaction mixture is cooled and concentrated in vacuo to a residue which is purified by chromatography on silica gel by elution with 2:1 ethyl acetate-hexanes to give 0.332 g of the desired product. FAB MASS SPEC 818 (M+H)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05292734
出典データセットuspto-grants-1994_03
ORD IDord-26d0b83d02794f3aa0d00199cec386d6
出典メモuspto-grants-1994_03