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HRID 1390920作成日:2026年10月27日
Propylene Oxide → 2-Amino-5-[1-hydroxy-2-[N-(1-methyl-3-phenylpropyl)-N-(phenylmethyl)amino]ethyl]benzenesulphonamide
https://huagongshe.com/reaction/1390920
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Propylene Oxide | HCID 6378 | — |
| 反応物 | N-benzyl-4-phenylbutan-2-amine | HCID 4362644 | — |
| 反応物 | 2-Amino-5-(2-bromoacetyl)benzenesulphonamide | HCID 12952403 | — |
| 溶媒 | Methyl Ethyl Ketone | HCID 6569 | — |
| 生成物 | 2-Amino-5-[1-hydroxy-2-[N-(1-methyl-3-phenylpropyl)-N-(phenylmethyl)amino]ethyl]benzenesulphonamide | HCID 12952416 | — |
反応手順
A solution of 2-amino-5-(2-bromoacetyl)benzenesulphonamide (0.5 g), N-(1-methyl-3-phenylpropyl)-N-(phenylmethyl) amine (0.45 g) and propylene oxide (2.5 ml) in 2-butanone (30 ml) was heated under reflux for 3 hours. The solution was then concentrated to a red-brown oil (0.7 g) which was dissolved in absolute ethanol (30 ml) and treated with sodium borohydride (258 mg) at room temperature during 2 hours. Excess borohydride was then destroyed with 2N hydrochloric acid and the ethanol was removed under reduced pressure. The residue was basified with 8% sodium bicarbonate and extracted with ethyl acetate (3 × 50 ml). The extracts were washed with water (100 ml), dried and concentrated to an orange oil (0.63 g). The oil was dissolved in acetone (10 ml) and re-precipitated as an orange solid (340 mg) by addition of petroleum ether (b.p. 60°-80°). Chromatographic purification of this solid on silica plates [Merck St17; elution with chloroform: methanol (5:1 )] and conversion of the product into a hydrochloride salt gave the title compound, 0.2 g, m.p. 133°-136°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04140713 |
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| 出典データセット | uspto-grants-1979_02 |
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| ORD ID | ord-2309abf70acc471fb65385e09488ab8f |
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| 出典メモ | uspto-grants-1979_02 |
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