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HRID 870037作成日:2026年10月26日

Tributylphosphine → 5-chloro-3-(3-chlorobenzyl)-N-[1-(4-cyanophenyl)ethyl]thiophene-2-carboxamide

https://huagongshe.com/reaction/870037

反応式

関与物質

役割名称HCID仕込み量
反応物TributylphosphineHCID 13831—
反応物Diphenyl diselenideHCID 15460—
反応物4'-CyanoacetophenoneHCID 74044—
反応物5-Chloro-3-(3-chlorobenzyl)thiophene-2-carboxylic acidHCID 45140204—
反応物4-(1-Azidoethyl)benzonitrileHCID 57900982—
溶媒AcetonitrileHCID 6342—
生成物5-chloro-3-(3-chlorobenzyl)-N-[1-(4-cyanophenyl)ethyl]thiophene-2-carboxamideHCID 57900981—

反応手順

To a suspension of 5-chloro-3-(3-chlorobenzyl)thiopbene-2-carboxylic acid from Example 1, Step 6 (230 mg, 0.801 mmol), 4-(1-azidoethyl)benzonitrile (146 mg, 0.848 mmol) [prepared according to Thompson et al. J. Org. Chem. 1993, 58, 5886, after reduction of commercially available 4-acetylbenzonitrile] and diphenyl diselenide (549 mg, 1.76 mmol) in acetonitrile at r.t. under N2 was added tributylphosphine (217 μL, 0.881 mmol, 1.1 eq) dropwise (suspension dissolved, slightly exothermic) and the mixture was stirred at r.t. for 6 h, quenched with saturated NaHCO3 and extracted with ether. The crude was purified by Combi Flash chromatography system (10-40% EtOAc/hexane) to give the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08969394B2
出典データセットuspto-grants-2015_03
ORD IDord-27512fc6ee68476f8bc87d3b9152fbd4
出典メモuspto-grants-2015_03