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HRID 416298作成日:2026年10月27日

Triethylamine → tert-Butyl 2-(5-formylthiophene-2-carboxamido)phenylcarbamate

https://huagongshe.com/reaction/416298

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
反応物N-(tert-Butoxycarbonyl)-1,2-phenylenediamineHCID 676311—
反応物5-Formyl-2-thiophenecarboxylic AcidHCID 818882—
溶媒DimethylformamideHCID 6228—
生成物tert-Butyl 2-(5-formylthiophene-2-carboxamido)phenylcarbamateHCID 5893064533.5%

反応手順

A solution of 5-formylthiophene-2-carboxylic acid (350 mg, 2.24 mmol), tert-butyl 2-aminophenylcarbamate (467 mg, 2.24 mmol) and triethylamine (470 μL, 340 mg, 3.36 mmol) and BOP (1.1 g, 2.68 mmol) in DMF (10 mL) was stirred at room temperature for 2 hours. The reaction mixture was concentrated and purified by flash chromatography using 25% EtOAc in hexanes as an eluent, yielding 260 mg (33%) of the title compound. 1H NMR (CDCl3) 9.95 (s, 1H), 9.7 (br. s, 1H), 7.84 (d, 1H, J=8.0 Hz), 7.74 (m, 2H), 7.15 (m, 2H), 6.72 (s, 1H), 1.56 (s, 9H). LRMS: (calc) 346.1; (found) 369.1 (M+Na)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08088805B2
出典データセットuspto-grants-2012_01
ORD IDord-ee460b9b649d4ae1a10c3f119c93cbb9
出典メモuspto-grants-2012_01