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1-Chloro-4-phenylbutan-2-one → 2-Amino-6-phenethyl-3,7-dihydropyrrolo[2,3-d]pyrimidin-4-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-Chloro-4-phenylbutan-2-one | HCID 10921160 | — |
| 反応物 | 2-Aminoisocytosine | HCID 135408763 | — |
| 生成物 | 2-Amino-6-phenethyl-3,7-dihydropyrrolo[2,3-d]pyrimidin-4-one | HCID 135479891 | 39% |
反応手順
FIG. 19 presents the method used to synthesize 2-amino-6-phenethyl-3,7-dihydro-pyrrolo[2,3-d]pyrimidin-4-one 9. Phenylpropanoyl chloride7 was reacted with CH2N2 in the presence of gaseous hydrogen chloride and ether to produce 1-chloro-4-phenyl-2-butanone 8. 1-chloro-4-phenyl-2-butanone 8 was reacted with 2,6-diamino-3H-pyrimidin-4-one 1 to produce 2-amino-6-phenethyl-3,7-dihydro-pyrrolo[2,3-d]pyrimidin-4-one 9 at a 39% yield.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06562969B1 |
| 出典データセット | uspto-grants-2003_05 |
| ORD ID | ord-6d4d9d7c49004208bdb0460f4f9d7e6f |
| 出典メモ | uspto-grants-2003_05 |