化工社化工社 化学情報印刷レポート · 研究参考用
HRID 15014作成日:2026年10月25日
p-Toluenesulfonic acid → 2-{6-[2-(2-Chlorophenyl)-5-(4-propoxyphenyl)-pyrrol-1ylmethyl]-2-nitro-pyridin-3-yloxy}-ethanol
https://huagongshe.com/reaction/15014
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | Chloroform | HCID 6212 | — |
| 反応物 | 1-(2-Chlorophenyl)-4-(4-propoxyphenyl)-butane-1,4-dione | HCID 16090339 | — |
| 反応物 | Acetic acid 2-(6-aminomethyl-2-nitropyridin-3-yloxy)-ethyl ester | HCID 59341182 | — |
| 溶媒 | 2-Methylphenethyl alcohol | HCID 88267 | — |
| 生成物 | 2-{6-[2-(2-Chlorophenyl)-5-(4-propoxyphenyl)-pyrrol-1ylmethyl]-2-nitro-pyridin-3-yloxy}-ethanol | HCID 59341200 | 32.6% |
反応手順
To a solution of 0.2 gm of acetic acid 2-(6-aminomethyl-2-nitropyridin-3-yloxy)-ethyl ester (0.8 mmol) in 3 mL of 5:1 toluene-ethanol was added 0.20 gm of 1-(2-chlorophenyl)-4-(4-propoxyphenyl)-butane-1,4-dione and 10 mg of p-TsOH. The reaction mixture stirred at 100° C. for 72 h. The reaction mixture was poured into 200 mL of CHCl3 and washed twice with water (100 mL), saturated brine, dried (Na2SO4), and the solvents removed under reduced pressure. The residue was purified by column chromatography using 4% methanol-chloroform as an eluent to give 100 mg (25% yield) of an oil. This was used without further purification or characterization.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07732457B2 |
|---|
| 出典データセット | uspto-grants-2010_06 |
|---|
| ORD ID | ord-54e07e9af4464f6988cfab1ed5303406 |
|---|
| 出典メモ | uspto-grants-2010_06 |
|---|