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HRID 1026974作成日:2026年10月27日

3-Amino-2-methylpyridine → 3-Ethoxycarbonyl-7-(2-methyl-3-pyridylamino)-6-(4-phenylpiperidine-1-carbonyl)pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/1026974

反応式

関与物質

役割名称HCID仕込み量
反応物3-Amino-2-methylpyridineHCID 572616—
反応物7-Chloro-3-ethoxycarbonyl-6-(4-phenylpiperidine-1-carbonyl)pyrazolo[1,5-a]pyrimidineHCID 86646290—
生成物3-Ethoxycarbonyl-7-(2-methyl-3-pyridylamino)-6-(4-phenylpiperidine-1-carbonyl)pyrazolo[1,5-a]pyrimidineHCID 6754043064.5%

反応手順

In the same manner as in Example 19, step 5 and using 7-chloro-3-ethoxycarbonyl-6-(4-phenylpiperidine-1-carbonyl)pyrazolo[1,5-a]pyrimidine (0.20 g, 0.48 mmol) obtained in Example 19, step 4 and 3-amino-2-methylpyridine (0.105 g, 0.97 mmol), the title compound (0.150 g, 64%) was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08729264B2
出典データセットuspto-grants-2014_05
ORD IDord-4259d052b1794dda83d09adbbe29265f
出典メモuspto-grants-2014_05