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HRID 37718作成日:2026年10月26日
Hydrochloric Acid → N-hydroxy-5-[(2-phenyl-4-thiazolyl)methoxy]-1-(phenylmethyl)-N,2-dimethyl-1H-indole-3-acetamide
https://huagongshe.com/reaction/37718
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Oxalyl chloride | HCID 65578 | — |
| 反応物 | N-methylhydroxylamine hydrochloride | HCID 77906 | — |
| 反応物 | 1-[(Phenyl)methyl]-2-methyl-5-[(2-phenyl-4-thiazolyl)methoxy]-1H-indole-3-acetic acid | HCID 15288028 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 溶媒 | Dimethylacetamide | HCID 31374 | — |
| 生成物 | N-hydroxy-5-[(2-phenyl-4-thiazolyl)methoxy]-1-(phenylmethyl)-N,2-dimethyl-1H-indole-3-acetamide | HCID 15288043 | 57% |
反応手順
A mixture of the compound of Example 40 (1.0 g, 2.13 mmol), methylene chloride (50 mL) and dimethylacetamide (0.15 mL) is cooled to 5° C. and with stirring, a solution of oxalyl chloride (0.45 mL, 5.3 mmol) in methylene chloride (10 mL) is added slowly. After stirring at room temperature for 30 minutes, the reaction mixture is poured into a solution containing tetrahydrofuran (11 mL), water (1.1 mL), triethylamine (1.8 mL) and N-methylhydroxylamine hydrochloride (0.7 g, 8.5 mmol). After stirring at room temperature for 1 hour, the reaction mixture is diluted with methylene chloride (150 mL), poured into 2N HCl (150 mL) and the layers are separated. The aqueous layer is washed again with methylene chloride (100 mL). The combined methylene chloride extract is washed with water (100 mL) and brine (100 mL), dried over MgSO4 and concentrated under reduced pressure to give 1.0 g of a crude solid. The solid is recrystallized from ether/methylene chloride to give 0.6 g of white crystalline product in 57 % yield, m.p. 171°-173° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05420289 |
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| 出典データセット | uspto-grants-1995_05 |
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| ORD ID | ord-8f69cf4c756f4fb8bd6d78b4fee31505 |
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| 出典メモ | uspto-grants-1995_05 |
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