関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Purine, 6-bromo- | HCID 5287830 | — |
| 反応物 | 1-(5-Chloro-2-(pyridin-2-yl)quinolin-3-yl)ethanamine | HCID 57707943 | — |
| 溶媒 | 1-Butanol | HCID 263 | — |
| 生成物 | N-(1-(5-Chloro-2-(pyridin-2-yl)quinolin-3-yl)ethyl)-9H-purin-6-amine | HCID 178463528 | 69% |
反応手順
Added 1-(5-chloro-2-(pyridin-2-yl)quinolin-3-yl)ethanamine (103 mg, 363 μmol), 6-bromopurine (72 mg, 363 μmol), n-butanol (2 mL) and DIPEA (190 μl, 1089 μmol) to a 10 mL flask. Submerged in an oil bath and heated at 110° C. for 40 h. The reaction mixture was concentrated on the rotavap to ˜0.5 mL of solvent, diluted with DCM, and chromatographed with 0-15% MeOH:DCM on 12 g silica gel column. The desired fractions were combined and concentrated to an oil which was dissolved in ACN:H2O and lyophilized to obtained 100 mg (69%) of a light tan solid. LC-MS (+esi, M+H+=402.1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08193199B2 |
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| 出典データセット | uspto-grants-2012_06 |
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| ORD ID | ord-47474595ce854c93baeb21b20aa0637d |
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| 出典メモ | uspto-grants-2012_06 |
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