関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cyclopentylamine | HCID 2906 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-Amino-4-chloropyrimidine | HCID 223332 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | N4-cyclopentylpyrimidine-2,4-diamine | HCID 58299890 | 84.5% |
反応手順
A mixture of 2-amino-4-chloropyrimidine (22.8 g, 176 mmol), cyclopentylamine (20.9 mL, 211 mmol) and triethylamine (29.4 mL, 211 mmol) in EtOH (200 mL) was heated at reflux (105° C., oil bath) for 48 h. Upon workup, the volatile was removed in vacuo. The residue was poured into ice and saturated Na2CO3 aqueous solution and extracted with ethyl acetate (3×). The combined organics were washed with saturated Na2CO3 aqueous solution (1×), dried over Na2SO4, and concentrated in vacuo to give N4-cyclopentylpyrimidine-2,4-diamine (315) (26.5 g) as a light yellow solid of 92% purity. This batch of material was taken onto the next step without further purification. LCMS-ESI (POS), M/Z, M+1: Found 179.1, Calculated 179.1.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08841312B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-50f69fdebf1f4b2284aa376c6e2cf73c |
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| 出典メモ | uspto-grants-2014_09 |
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