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HRID 126809作成日:2026年10月26日
Dicyclohexylcarbodiimide → 5,5-Dimethyl-8-(3-methyl-2-octyl)-10-[4-(piperidino)butyryloxy]-5H-[1]benzopyrano[3,4-d]pyridine hydrochloride
https://huagongshe.com/reaction/126809
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 反応物 | 4-(Piperidin-1-yl)butanoic acid hydrochloride | HCID 13172081 | — |
| 反応物 | 5,5-Dimethyl-10-hydroxy-8-(3-methyl-2-octyl)-5H-[1]benzopyrano[3,4-d]pyridine | HCID 19781402 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 5,5-Dimethyl-8-(3-methyl-2-octyl)-10-[4-(piperidino)butyryloxy]-5H-[1]benzopyrano[3,4-d]pyridine hydrochloride | HCID 20287832 | — |
反応手順
A mixture of 3.53 g. (0.01 mole) of 5,5-dimethyl-10-hydroxy-8-(3-methyl-2-octyl)-5H-[1]benzopyrano[3,4-d]pyridine, 2.07 g. (0.01 mole) of γ-piperidinobutyric acid hydrochloride, 2.16 g. (0.0105 mole) of N,N'-dicyclohexylcarbodiimide, and 160 ml. of dried methylene chloride was stirred overnight at room temperature. The reaction mixture was cooled at approximately 5° C. for several hours and was filtered to remove dicyclohexylurea. The filtrate was evaporated in vacuo and the residue was dissolved in 12.5 ml. of methylene chloride and 50 ml. of cyclohexane. After standing overnight in the cold room (approximately 5° C.), the mixture was filtered again and the filtrate was evaporated in vacuo. The residue was recrystallized from methylene chloride/ether, giving 4.1 g. of the product, m.p. 134°-137°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04254116 |
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| 出典データセット | uspto-grants-1981_03 |
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| ORD ID | ord-d02bd2eb72254743b2fa2e02d4c6c99e |
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| 出典メモ | uspto-grants-1981_03 |
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