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HRID 68849作成日:2026年10月24日

2-Chloro-5-ethylpyrimidine → N-Cyclopropyl-N-[1-(5-ethyl-pyrimidin-2-yl)-3-methyl-piperidin-4-yl]-4-oxazol-5-yl-benzamide

https://huagongshe.com/ja/reaction/68849

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chloro-5-ethylpyrimidineHCID 3572763—
反応物HCID 68290188HCID 68290188—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物N-Cyclopropyl-N-[1-(5-ethyl-pyrimidin-2-yl)-3-methyl-piperidin-4-yl]-4-oxazol-5-yl-benzamideHCID 68351874—

反応手順

The title compound is prepared from N-cyclopropyl-N-(3-methyl-piperidin-4-yl)-4-oxazol-5-yl-benzamide and 2-chloro-5-ethyl-pyrimidine following a procedure analogous to that described in Example 19 using N-methylpyrrolidinone as solvent. LC (method 3): tR=1.83 min; Mass spectrum (ESI+): m/z=432 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822471B2
出典データセットuspto-grants-2014_09
ORD IDord-8ff19b4de1b04a52abe88db08cbe8a5c
出典メモuspto-grants-2014_09