戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 639262作成日:2026年10月26日

2,3-Dihydro-1,4-benzodioxin-6-methylamine → N-(2,3-Dihydro-1,4-benzodioxin-6-ylmethyl)-10-[(2-methoxy-2'-methyl-1,1'-biphenyl-4-YL)carbonyl]-10,11-dihydro-5H-pyrrolo[2,1-C][1,4]benzodiazepine-3-carboxamide

https://huagongshe.com/reaction/639262

反応式

関与物質

役割名称HCID仕込み量
反応物2,3-Dihydro-1,4-benzodioxin-6-methylamineHCID 87102—
反応物2,2,2-Trichloro-1-{10-[(2-methoxy-2'-methyl-1,1'-biphenyl-4-yl)carbonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-3-yl}ethanoneHCID 16038825—
生成物N-(2,3-Dihydro-1,4-benzodioxin-6-ylmethyl)-10-[(2-methoxy-2'-methyl-1,1'-biphenyl-4-YL)carbonyl]-10,11-dihydro-5H-pyrrolo[2,1-C][1,4]benzodiazepine-3-carboxamideHCID 16039138—

反応手順

The title compound was prepared in the manner of Example 36 from 2,2,2-trichloro-1-{10-[(2-methoxy-2′-methyl-1,1′-biphenyl-4-yl)carbonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-3-yl}ethanone of Example 35 and C-(2,3-dihydrobenzo[1,4]dioxin-6-yl)-methylamine. Purification was performed using HPLC with a normal phase column and eluting with a two phase solvent system (A=hexane, B=dichloromethane/methanol, 4:1), m.p. 153-155° C. MS [(+)ESI, m/z]: 600 [M+H]+

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07691848B2
出典データセットuspto-grants-2010_04
ORD IDord-884dbebd4b9e402a8a079d25e04ed865
出典メモuspto-grants-2010_04