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HRID 2234411作成日:2026年10月27日
Triethylamine → 10-Chloro-2-(3-furylmethyl)-6-methyl-2,6,9,11-tetrazabicyclo[5.4.0]undeca-7,9,11-trien-5-one
https://huagongshe.com/reaction/2234411
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 1-(Furan-3-yl)methanamine | HCID 2776197 | — |
| 反応物 | N-(2,4-dichloropyrimidin-5-yl)-N-methyl-prop-2-enamide | HCID 86617580 | — |
| 触媒 | Titanium tetraethoxide | HCID 76524 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 10-Chloro-2-(3-furylmethyl)-6-methyl-2,6,9,11-tetrazabicyclo[5.4.0]undeca-7,9,11-trien-5-one | HCID 86617581 | 15.3% |
反応手順
3-Furylmethylamine (Maybridge; 175 mg, 1.8 mmol), N-(2,4-dichloropyrimidin-5-yl)-N-methyl-prop-2-enamide (Intermediate 113; 347 mg, 1.5 mmol), Triethylamine (420 μL, 3 mmol), Titanium Tetra-ethoxide (157 μL, 0.75 mmol) and DCM (5 mL) were combined and stirred at room temp for 1 hr, heated at 40° C. overnight then cooled to room temperature. The reaction mixture was washed with water then gravity filtered through a PTFE cup, the aqueous layer containing the titanium emulsion was washed with further DCM (3×10 mL) and the combined organic solutions gravity filtered through a PTFE cup and solvents evaporated. The residue was dissolved in DCM and purified by chromatographic separation on silica eluting with a shallow gradient (25 column volumes) of 10-50% Ethyl Acetate/iso-hexane. Product containing fractions were combined and evaporated to give the title compound as a yellow gum (67 mg, 15%)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07709471B2 |
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| 出典データセット | uspto-grants-2010_05 |
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| ORD ID | ord-b1e0e6425e64402598d0e032e30bea48 |
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| 出典メモ | uspto-grants-2010_05 |
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