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HRID 872297作成日:2026年10月25日
4-Methoxy-2-pyrimidinamine → tert-butyl N-[1-[4-(7-oxo-3-phenyl-1H-imidazo[1,2-a]pyrimidin-2-yl)phenyl]cyclobutyl]carbamate
https://huagongshe.com/reaction/872297
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Methoxy-2-pyrimidinamine | HCID 67428 | — |
| 反応物 | tert-Butyl (1-{4-[bromo(phenyl)acetyl]phenyl}cyclobutyl)carbamate | HCID 86691038 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | tert-butyl N-[1-[4-(7-oxo-3-phenyl-1H-imidazo[1,2-a]pyrimidin-2-yl)phenyl]cyclobutyl]carbamate | HCID 178452600 | — |
反応手順
A mixture of crude {1-[4-(2-bromo-2-phenyl-acetyl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester [Int-1-A] (1.26 g) and 4-methoxypyrimidin-2-ylamine (0.67 g) in DMF (21 mL) was heated overnight at 90° C. (bath temperature). On cooling the mixture was partitioned between EtOAc and water and the organic phase washed with brine, dried and concentrated to give a mixture of the title compound and Int-2-0. Purification was achieved by preparative HPLC 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 | US08975265B2 |
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| 出典データセット | uspto-grants-2015_03 |
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| ORD ID | ord-f7044b18d69d4fd0b4a5a19715df59e5 |
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| 出典メモ | uspto-grants-2015_03 |
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