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HRID 2115014作成日:2026年10月25日

Phenyl-piperidin-4-yl-methanol → 2-[4-(Hydroxy-phenyl-methyl)-piperidin-1-yl]-2-oxo-N-(3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yl)-acetamide

https://huagongshe.com/reaction/2115014

反応式

関与物質

役割名称HCID仕込み量
反応物Phenyl-piperidin-4-yl-methanolHCID 339086—
反応物N-(3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yl)-oxalamic acidHCID 69100554—
溶媒Diethyl EtherHCID 3283—
生成物2-[4-(Hydroxy-phenyl-methyl)-piperidin-1-yl]-2-oxo-N-(3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yl)-acetamideHCID 69100812—

反応手順

The title compound is prepared from N-(3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-7-yl)-oxalamic acid (Example 53b) and phenyl-piperidine-4-yl-methanol [J. Amer. Chem. Soc.,52, 4006. (1930)] according to the method described in Example 1c. Melting Point: 195-197° C. (diethylether)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07435744B2
出典データセットuspto-grants-2008_10
ORD IDord-2fc867673e2f4b2d934fd7e99e0e3b4d
出典メモuspto-grants-2008_10