関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | Ethylenediamine | HCID 3301 | — |
| 反応物 | 2-Chloropyridine | HCID 7977 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | N~1~-(Pyridin-2-yl)ethane-1,2-diamine | HCID 410428 | — |
| 反応物 | HCID 178512433 | HCID 178512433 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 4-(2-{[2-(2-Pyridylamino)ethyl]amino}pyrimidin-4-yl)benzamide | HCID 22142834 | — |
反応手順
2-(2-Aminoethylamino)pyridine (prepared from 2-chloropyridine and ethylenediamine in accordance with the method described in T. Mega et al., 1988, Bull. Chem. Soc. Japan 61:4315, which is incorporated herein by reference) (6 mmol) was treated with benzotriazole carboxamidinium 4-methylbenzenesulfonatesulfonate (2.0 g, 6 mmol) and DIEA (1.05 ml, 6 mmol) in anhydrous acetonitrile (10 ml) for 65 hours. Ether (ca. 10 ml) was then added to this mixture. After 8 hours the white solid amino[2-(2-pyridylamino)ethyl]carboxamidinium 4-methylbenzenesulfonate was filtered off and dried in vacuo. The resulting guanidine (200 mg) was reacted with 100 mg of resin (21 hours, 90° C.) according to the method described in Example 10 (Resin method C), to give the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07425557B2 |
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| 出典データセット | uspto-grants-2008_09 |
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| ORD ID | ord-c5bdf6da68cb40abbb85507f429e9fe9 |
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| 出典メモ | uspto-grants-2008_09 |
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