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HRID 343343作成日:2026年10月26日
Sodium hydride → 2-(2-oxopyrrolidin-1-yl)-N-(3-methyl-5,6,7,8-tetrahydrothieno[2,3-b]quinolin-4-yl)acetamide
https://huagongshe.com/reaction/343343
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Methyl 2-oxo-1-pyrrolidineacetate | HCID 108835 | — |
| 反応物 | 4-Amino-3-methyl-5,6,7,8-tetrahydrothieno[2,3-b]quinoline | HCID 15225118 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | 2-(2-oxopyrrolidin-1-yl)-N-(3-methyl-5,6,7,8-tetrahydrothieno[2,3-b]quinolin-4-yl)acetamide | HCID 15385071 | — |
反応手順
Into a suspension of 1.26 g of sodium hydride (60% content) in 15 ml of N-methylpyrrolidone, was added 3.28 g of 4-amino-3-methyl-5,6,7,8-tetrahydrothieno[2,3-b]quinoline at room temperature. The mixture was heated to 50° C. and stirred for 40 minutes. Thereafter, 4.72 g of methyl 2-oxo-1-pyrrolidine acetate was added dropwise to the mixture at 50° C. over a period of 30 minutes. After the stirrng at 50° C. for 20 minutes, the mixture was cooled to 15° C. and poured into 130 ml aqueous solution containing 13.5 g of ammonium chloride.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05861411 |
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| 出典データセット | uspto-grants-1999_01 |
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| ORD ID | ord-8ef3663b434044298bab24f903f6e607 |
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| 出典メモ | uspto-grants-1999_01 |
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