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HRID 23658作成日:2026年10月25日
Diisopropylethylamine → N-(4-chlorobenzyl)-2-{[[2-(2,6-dimethoxyphenyl)-2-hydroxyethyl](methyl)amino]methyl}-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide
https://huagongshe.com/reaction/23658
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | N-(4-chlorobenzyl)-2-(chloromethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide | HCID 22574363 | — |
| 反応物 | 1-(2,6-Dimethoxyphenyl)-2-(methylamino)ethan-1-ol | HCID 22574395 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | N-(4-chlorobenzyl)-2-{[[2-(2,6-dimethoxyphenyl)-2-hydroxyethyl](methyl)amino]methyl}-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide | HCID 22574406 | 52.6% |
反応手順
A mixture of N-(4-chlorobenzyl)-2-(chloromethyl)-3,4-dimethyl-7-oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamide (50 mg, 0.13 mmol), 1-(2,6-dimethoxyphenyl)-2-(methylamino)ethanol (PNU-149291, Arch. Intern. Pharmacodyn. 1965, 154, 26-39) (42 mg, 0.20 mmol) and diisopropylethylamine (34 μL, 0.20 mmol) in dry DMF (2.7 mL) was heated to 60° C., becoming a solution. The reaction was stirred for 7 hours at that temperature. After cooling to room temperature, the solution was diluted with water (7 mL). The resulting milky suspension was stirred vigorously for 30 minutes, and then left standing overnight at room temp. The mixture was filtered, and the collected solid was washed with water and dried in vacuo, leaving a white solid. Recrystallization from acetonitrile (10 mL, dissolved with warming and then cooled to 0° C. overnight) gave the title compound (39 mg) as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06852731B2 |
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| 出典データセット | uspto-grants-2005_02 |
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| ORD ID | ord-797449f7fa6946f490124dbc304acff7 |
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| 出典メモ | uspto-grants-2005_02 |
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