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Acetic Acid → 8-Cyclopentyl-2-[[4-(morpholin-4-yl)phenyl]amino]-8H-pteridin-7-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Ethyl (3,5-dimethoxyphenyl)(oxo)acetate | HCID 24722256 | — |
| 反応物 | 5-Amino-2-[[4-[2-(diethylamino)-ethoxy]phenyl]amino]-4-(ethylamino)pyrimidine pyrimidine | HCID 69475532 | — |
| 生成物 | 8-Cyclopentyl-2-[[4-(morpholin-4-yl)phenyl]amino]-8H-pteridin-7-one | HCID 9865314 | 56% |
反応手順
A mixture of 0.96 g (2.8 mmol) of 5-amino-2-[[4-[2-(diethylamino)-ethoxy]phenyl]amino]-4-(ethylamino)pyrimidine pyrimidine, 0.83 g (35 mmol) of ethyl 2-(3,5-dimethoxyphenyl)-2-oxoacetate (from Example 4(2)), and 1 mL of acetic acid in 25 mL EtOH is heated under reflux for 14 hours, and the solvent is removed under vacuum. The residue is then dissolved in water and washed with EtOAc. The aqueous layer is made basic with aqueous ammonia, and the crude product is extracted into fresh EtOAc. Chromatography on alumina, eluting with hexane/EtOAc (1:1), then gives 0.81 g (56%) of the title compound (Compound 14): mp (MeOH) 154–155° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07169778B2 |
| 出典データセット | uspto-grants-2007_01 |
| ORD ID | ord-4be740f3229043b18e7d5db8aea88064 |
| 出典メモ | uspto-grants-2007_01 |