戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 361812作成日:2026年10月26日

1-benzyl-N-methylpiperidin-4-amine → U 99363

https://huagongshe.com/reaction/361812

反応式

関与物質

役割名称HCID仕込み量
反応物1-benzyl-N-methylpiperidin-4-amineHCID 4136128—
反応物2-Bromo-3-ethoxypyridineHCID 10631926—
溶媒DichloromethaneHCID 6344—
生成物U 99363HCID 133107—

反応手順

A mixture of 1-benzyl-4-(methylamino)piperidine (EXAMPLE 9, 2.92 g) and 2-bromo-3-ethoxypyridine (EXAMPLE 69, 1.44 g) is stirred at 160°-165° in a sealed tube for 2 days, diluted with methylene chloride (50 ml), washed with water (10 ml) and saline (10 ml), dried over sodium sulfate, and concentrated under reduced pressure. The residue is chromatographed on silica gel (230-400 mesh, 300 g; eluting with a gradient of ethyl acetate/hexane (10/90-50/50)) to give the title compound, C,H,N: Anal. Calcd for C20H27N3O1 : C=73.81, H=8.36, N=12.91-found: C=73.59, H=8.37, N=12.83.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05866589
出典データセットuspto-grants-1999_02
ORD IDord-f46c67e942b3493db6a54f5c40fb808f
出典メモuspto-grants-1999_02