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HRID 890804作成日:2026年10月26日

Methyl 5-bromothiophene-2-carboxylate → 5-(3-tert-Butoxycarbonylamino-prop-1-ynyl)-thiophene-2-carboxylic Acid Methyl Ester

https://huagongshe.com/reaction/890804

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 5-bromothiophene-2-carboxylateHCID 605713—
反応物tert-butyl N-(prop-2-yn-1-yl)carbamateHCID 11073648—
触媒TriethylamineHCID 8471—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
生成物5-(3-tert-Butoxycarbonylamino-prop-1-ynyl)-thiophene-2-carboxylic Acid Methyl EsterHCID 5407533963,406.199%

反応手順

A mixture of prop-2-ynyl-carbamic acid tert-butyl ester (1.67 g, 0.011 mmol), 5-bromo-thiophene-2-carboxylic acid methyl ester (2.50 g, 0.011 mmol), tetrakistriphenylphosphine(0) palladium (0.622 g, 0.0538 mmol), Cul (0.102 g, 0.538 mmol) and triethylamine (1.57 mL, 0.011 mmol) in 50 mL acetonitrile under nitrogen was heated at reflux for 16 h. The reaction was cooled to room temperature, diluted with 75 mL EtOAc, washed with 5.5% HCl, water and brine, dried over MgSO4, filtered and concentrated in vacuo to an oil. The product was purified via flash chromatography (9:1 to 4:1 hexanes:EtOAc) to afford the title compound as an oil (2.06 g). MS 313 (M+18).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06998423B2
出典データセットuspto-grants-2006_02
ORD IDord-b56a5b6057d54f95ba3d316ea5a51b4b
出典メモuspto-grants-2006_02