戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 22904作成日:2026年10月25日

(2-Thienylmethyl)amine → 3-(3,5-Dichloro-2-hydroxyphenyl)-3-{(5-oxo-1-(3-{((2-thienylmethyl)amino)carbonylamino}phenyl)pyrrolidin-3-yl)carbonylamino}propanoic acid

https://huagongshe.com/reaction/22904

反応式

関与物質

役割名称HCID仕込み量
反応物(2-Thienylmethyl)amineHCID 34005—
反応物3-(3-Fluorophenyl)-3-{(5-oxo-1-(3-{(benzylamino)carbonylamino}phenyl)pyrrolidin-3-yl)carbonylamino}propanoic acidHCID 22591754—
反応物Ethyl 3-amino-3-(3,5-dichloro-2-hydroxyphenyl)propanoateHCID 22591801—
生成物3-(3,5-Dichloro-2-hydroxyphenyl)-3-{(5-oxo-1-(3-{((2-thienylmethyl)amino)carbonylamino}phenyl)pyrrolidin-3-yl)carbonylamino}propanoic acidHCID 10167402—

反応手順

The title compound was analogously synthesized to the preparation of 3-(3-fluorophenyl)-3-{(5-oxo-1-(3-{(benzylamino)carbonylamino}phenyl)pyrrolidin-3-yl)carbonylamino}propanoic acid from ethyl 3-amino-3-(3,5-dichloro-2-hydroxyphenyl)propanoate and 2-thienylmethyl amine. MS (ES+): 591 (M+H)+; (ES−): 589 (M−H)−.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06849639B2
出典データセットuspto-grants-2005_02
ORD IDord-2dcac970ba41443aa25c723595a5a9dc
出典メモuspto-grants-2005_02