戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 573064作成日:2026年10月26日

Triethylamine → (Z)-tert-butyl 5-(benzyloxy)-3-(3-morpholino-3-oxoprop-1-enyl)-1H-indole-1-carboxylate

https://huagongshe.com/reaction/573064

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Tri-o-tolylphosphineHCID 80271—
反応物AcryloylmorpholineHCID 98723—
反応物5-(Benzyloxy)-3-bromo-1H-indole, N-BOC protectedHCID 40428554—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
溶媒Ammonium ChlorideHCID 25517—
生成物(Z)-tert-butyl 5-(benzyloxy)-3-(3-morpholino-3-oxoprop-1-enyl)-1H-indole-1-carboxylateHCID 67227351—

反応条件

温度100 °C

反応手順

A mixture of tert-butyl 5-(benzyloxy)-3-bromo-1H-indole-1-carboxylate (2.011 g), 1-morpholinoprop-2-en-1-one (0.776 g), palladium acetate (31 mg), tri-o-tolylphosphine (187 mg) and triethylamine (1.14 mL) in N,N-dimethylformamide (14 mL) under nitrogen atmosphere was stirred at 100° C. overnight. The mixture was diluted with ethyl acetate and saturated ammonium chloride. The aqueous layer was extracted with ethyl acetate and the combined organic layers were dried over MgSO4, filtered and concentrated. The residue was purified by flash chromatography (80% ethyl acetate-hexane) to give the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09029404B2
出典データセットuspto-grants-2015_05
ORD IDord-73b57b0cfd00485b8716c6d5aa974531
出典メモuspto-grants-2015_05