関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | (Quinolin-2-yl)methanamine dihydrochloride | HCID 18507294 | — |
| 反応物 | Trifluoromethanesulfonic acid 2-amino-6-furan-2-yl-5-methyl-pyrimidin-4-yl ester | HCID 86583753 | — |
| 溶媒 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 生成物 | 4-Chloro-6-(2-furyl)-5-methylpyrimidine-2-amine | HCID 18507243 | 50% |
反応手順
To a stirred solution of 250 mg (0.77 mmol) trifluoromethanesulfonic acid 2-amino-6-furan-2-yl-5-methyl-pyrimidin-4-yl ester in 10 ml DME was added 489 mg (2.12 mmol) 2-(aminomethyl)quinoline dihydrochloride and the mixture heated at 80° C. for 16 hours. The reaction mixture was then concentrated in vacuo. Chromatography (ethyl acetate/hexane 4/1) followed by trituration in ether/hexane afforded 80 mg (50%) 4-chloro-6-furan-2-yl-5-methyl-pyrimidin-2-ylamine as a white crystalline solid. ES-MS m/e (%): 212 (M{37Cl}+H+, 50), 210 (M{35Cl}+H+, 100).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06586441B2 |
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| 出典データセット | uspto-grants-2003_07 |
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| ORD ID | ord-c977743f553b4ed087bc3a24d77fb843 |
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| 出典メモ | uspto-grants-2003_07 |
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