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HRID 325884作成日:2026年10月27日
Phosgene → 5,10-Dihydro-5-{[(1-methyl-4-piperidinyl)oxy]carbonyl}-11H-dibenzo[b,e][1,4]diazepin-11-one
https://huagongshe.com/reaction/325884
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Phosgene | HCID 6371 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 4-Piperidinol, 1-methyl- | HCID 66048 | — |
| 反応物 | 5,10-Dihydro-11H-dibenzo(b,e)(1,4)diazepin-11-one | HCID 201327 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 5,10-Dihydro-5-{[(1-methyl-4-piperidinyl)oxy]carbonyl}-11H-dibenzo[b,e][1,4]diazepin-11-one | HCID 13276748 | — |
反応手順
A quantity of 4.9 gm (0.0425 mol) of 1-methyl-4-piperidinol was added dropwise to a mixture of 22.5 ml of a 20% solution of phosgene in toluene, 100 ml of dioxane, and 4.75 gm (0.045 mol) of anhydrous sodium carbonate while external cooling with ice was carried out. The mixture was stirred for a further 60 minutes at ambient temperature, 9.0 gm (0.0428 mol) of 5,10-dihydro-11H-dibenzo[b,e][1,4]diazepin-11-one were added to the reaction mixture, and this was then refluxed for four hours. The mixture was filtered, the filtrate was concentrated by evaporation in vacuo, and the crude product obtained was purified by column chromatography on 500 gm of silica gel [eluant: ethyl acetate/methanol (volume ratio of 10:1)]. After recrystallization from ethyl acetate, the resulting colorless crystals melted at 203°-204° C. and were identical--according to the mixed melting point, thin layer chromatogram, and IR spectrum--to a product prepared according to Example 4. Yield: 7.6 gm (51% of theory).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04443452 |
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| 出典データセット | uspto-grants-1984_04 |
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| ORD ID | ord-0175f5fc7cb344e9ae00fa40432413e2 |
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| 出典メモ | uspto-grants-1984_04 |
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