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HRID 36220作成日:2026年10月25日

alpha,4-Dichloroanisole → 5-n-Butyl-2-(4-chlorophenoxymethyl)-2,4-dihydro-4-[[2'-(N-trityltetrazol-5-yl)biphenyl-4-yl]methyl]-3H-1,2,4-triazol-3-one

https://huagongshe.com/reaction/36220

反応式

関与物質

役割名称HCID仕込み量
反応物alpha,4-DichloroanisoleHCID 88801—
反応物5-n-Butyl-2,4-dihydro-4-[[2'-(N-trityltetrazol-5-yl)biphenyl-4-yl]methyl]-3H-1,2,4-triazol-3-oneHCID 19939386—
生成物5-n-Butyl-2-(4-chlorophenoxymethyl)-2,4-dihydro-4-[[2'-(N-trityltetrazol-5-yl)biphenyl-4-yl]methyl]-3H-1,2,4-triazol-3-oneHCID 1993950755%

反応手順

The alkylation of 5-n-butyl-2,4-dihydro-4-[[2'-(N-trityltetrazol-5-yl)biphenyl-4-yl]methyl]-3H-1,2,4-triazol-3-one (from Example 2, Step D) with α,4-dichloroanisole was carried out as described in Example 3, Step A, except that only 5 equivalents of the alkylating agent was used. After work-up, the residue was flash chromatographed over silica gel (25 mL for 0.162 mmole, gradient elution using 0.25-1.0% MeOH/CH2Cl2) to give the desired material as a colorless oil in 55% yield, homogeneous by TLC in 2% MeOH/CH2Cl2, mass spectrum (FAB) 758 (M+1)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05411980
出典データセットuspto-grants-1995_05
ORD IDord-e0e86bf8405e4202baa3105b58509213
出典メモuspto-grants-1995_05