戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 609598作成日:2026年10月26日

Cyclohexane, (bromomethyl)- → N-[(1-Cyclohexylmethyl-4-piperidyl)methyl] 3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carboxamide

https://huagongshe.com/reaction/609598

反応式

関与物質

役割名称HCID仕込み量
反応物Cyclohexane, (bromomethyl)-HCID 137636—
反応物N-(4-Piperidylmethyl) 3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carboxamideHCID 9839803—
生成物N-[(1-Cyclohexylmethyl-4-piperidyl)methyl] 3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carboxamideHCID 19599430—

反応手順

N-(4-Piperidylmethyl) 3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carboxamide (E21) was alkylated with cyclohexylmethyl bromide using the method of Example 22 with a reaction time of 70 h at room temperature followed by 8 h at reflux temperature. The title compound (E23) was obtained as a white solid (31%) which was converted to its hydrochloride salt and crystallised from acetone/ether as a white solid mp 209-210° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05998409
出典データセットuspto-grants-1999_12
ORD IDord-be72e82c748c4a63a48e064a2ee2236f
出典メモuspto-grants-1999_12