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HRID 656660作成日:2026年10月27日
1,3-Dioxolane-4-methanol → 3-Amino-5-chloro-6-([1,3]dioxolan-4-ylmethoxy)-4-methyl-thieno[2,3-b]pyridine-2-carboxylic acid cyclopropylamide
https://huagongshe.com/reaction/656660
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,3-Dioxolane-4-methanol | HCID 21618 | — |
| 反応物 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 反応物 | 3-Amino-5-chloro-6-methanesulfinyl-4-methyl-thieno[2,3-b]pyridine-2-carboxylic acid cyclopropylamide | HCID 57664420 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3-Amino-5-chloro-6-([1,3]dioxolan-4-ylmethoxy)-4-methyl-thieno[2,3-b]pyridine-2-carboxylic acid cyclopropylamide | HCID 57664421 | 51% |
反応手順
To a solution of glycerol formal (0.729 g, 7.0 mmol) in THF (3 ml) at room temperature is added dropwise a solution of lithium bis(trimethylsilyl)amide (1.0 M in hexanes)(3.50 ml, 3.50 mmol). The reaction mixture is stirred for 15 minutes and then is treated with 3-amino-5-chloro-6-methanesulfinyl-4-methyl-thieno[2,3-b]pyridine-2-carboxylic acid cyclopropylamide (0.345 g, 1.00 mmol). The reaction mixture is heated at 75° C. in a sealed tube for 1.5 hours, cooled to room temperature, and then quenched by the addition of water (10 ml). The reaction mixture is transferred to an erlenmeyer flask and diluted to 75 ml with water. The mixture is cooled to 0° C. and stirred. During this time, a white precipitate is formed. This solid is collected by filtration and slurried in a 2:1 EtOAc:hexane mixture. This slurry is stirred for 10 minutes, filtered, and the collected solid is placed in the vacuum oven to dry (60° C. for 16 hours). This affords the title compound as a white solid (0.195 g, 51%). Mass (m/z): 384.1 (M++1), 382.1 (M+−1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08071776B2 |
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| 出典データセット | uspto-grants-2011_12 |
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| ORD ID | ord-1e68c9412ca04864b8f2ee997b02c5aa |
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| 出典メモ | uspto-grants-2011_12 |
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