関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 反応物 | 4-Benzyloxy-3-chloroaniline | HCID 1268285 | — |
| 反応物 | 4-chloro-5H-pyrrolo[3,2-d]pyrimidine | HCID 5370695 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | N-[4-(benzyloxy)-3-chlorophenyl]-5H-pyrrolo[3,2-d]pyrimidin-4-amine | HCID 57597271 | 49.5% |
反応手順
A mixture of 4-chloro-5H-pyrrolo[3,2-d]pyrimidine (200 mg), 4-(benzyloxy)-3-chloroaniline (365 mg) and 1-methyl-2-pyrrolidone (3 mL) was stirred at 80° C. for 4 hrs. Methanol and activated carbon were added to the reaction mixture and the mixture was stirred. The activated carbon was filtered off, aqueous sodium hydrogen carbonate solution was added and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (eluent, methanol:ethyl acetate=0:100→15:75) and recrystallized from ethanol-ethyl acetate to give the title compound (226 mg) as a pale-brown powder.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07507740B2 |
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| 出典データセット | uspto-grants-2009_03 |
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| ORD ID | ord-69cd76e25f794ae5ae52dfdfac3d9ec8 |
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| 出典メモ | uspto-grants-2009_03 |
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