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HRID 1713037作成日:2026年10月25日

Triethylamine → HCID 11582303、化合物

https://huagongshe.com/reaction/1713037

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ethyl 4-isocyanatobutyrateHCID 3445674—
反応物2-(4-nitro-phenyl)-4H-furo[3,2-b]pyrrole-5-carboxylic acid ethyl esterHCID 59463445—
反応物HCID 86618327HCID 86618327—
反応物4-IsocyanatobutyrateHCID 86618337—
溶媒HexaneHCID 8058—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 11582303HCID 1158230374%

反応手順

2-(4-Nitro-phenyl)-4H-furo[3,2-b]pyrrole-5-carboxylic acid ethyl ester (25 mg, 0.087 mmol, 1 molequivalent), prepared as described hereinabove (see, preparation of Compound 1), ethyl 4-isocyanatobutyrate (135 mg, 0.87 mmol) and triethylamine (214 μl, 1.74 mmol) were stirred overnight at room temperature. Additional 4-isocyanatobutyrate (130 μl) was added and the mixture was heated to 50° C. and was stirred at this temperature overnight. Once TLC analysis, using a 2:1 hexane:ethyl acetate mixture as eluent, indicated a complete conversion, the crude mixture was purified by column chromatography using a gradient of hexane to hexane:ethyl acetate (9:1) as eluent to give pure Compound 30 (26 mg, 74% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07795255B2
出典データセットuspto-grants-2010_09
ORD IDord-e4a13dcc3813461088139e50413ed0c5
出典メモuspto-grants-2010_09