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HRID 1363301作成日:2026年10月25日

Triethylamine → 4-tert-butoxycarbonyl-4H-furo[3,2-b]pyrrole-5-carboxylic acid methyl ester

https://huagongshe.com/reaction/1363301

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Di-tert-butyl dicarbonateHCID 90495—
反応物methyl 4H-furo[3,2-b]pyrrole-5-carboxylateHCID 5082263—
反応物Ethyl acetate hexaneHCID 21226206—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物4-tert-butoxycarbonyl-4H-furo[3,2-b]pyrrole-5-carboxylic acid methyl esterHCID 5964860362%

反応手順

To a solution of methyl 4H-furo[3,2-b]pyrrole-5-carboxylate (1.0 g, 6.06 mmol) in CH2Cl2 (10 ml) was added triethyl amine (1.85 g, 18.2 mmol) and DMAP (148 mg 1.22 mol). Then BOC2O (2.0 g, 9.1 mmol) was added. The resulting mixture was stirred overnight. After the reaction was complete as judged TLC analysis (10% EtOAc/hexane), the reaction mixture was washed with water and brine and dried over Na2SO4. After filtration, the filtrate was concentrated and the crude product was purified by silica gel chromatography (20% EtOAc in hexane) to give 4-tert-butoxycarbonyl-4H-furo[3,2-b]pyrrole-5-carboxylic acid methyl ester as a white solid (987 mg, 62%). 1H NMR (400 MHz, CDCl3) δ (ppm) 7.45 (d, J=1.47 Hz, 1H), 6.82 (s, 1H), 6.59 (s, 1H), 3.80 (s, 3H), 1.55 (s, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07884124B2
出典データセットuspto-grants-2011_02
ORD IDord-19c654556d1c4c8e9feb0d3ef25eceef
出典メモuspto-grants-2011_02