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HRID 2292903作成日:2026年10月27日

Ethyl Acetate → 2-[(2-bromo)acetyl]amino-3-(1H-indol-3-yl)1-[N-(2-methoxybenzyl)acetylamino]propane

https://huagongshe.com/reaction/2292903

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Bromoacetyl bromideHCID 61147—
反応物DiisopropylethylamineHCID 81531—
反応物2-amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propaneHCID 22508955—
溶媒TetrahydrofuranHCID 8028—
生成物2-[(2-bromo)acetyl]amino-3-(1H-indol-3-yl)1-[N-(2-methoxybenzyl)acetylamino]propaneHCID 69736949—

反応手順

To a stirring solution of 2-amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propane (7.51 g, 21.369 mmoles) in anhydrous tetrahydrofuran (100 ml) under a nitrogen atmosphere at 0° C. was added diisopropylethylamine (4.1 ml, 23.537 mmoles) and bromoacetyl bromide (2.05 ml, 23.530 mmoles). After 2 hours, ethyl acetate was added and the reaction mixture washed with water twice, 1.0N hydrochloric acid (2×), saturated sodium bicarbonate solution (2×), and brine. The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated to a tan foam on a rotary evaporator. In this manner the 2-[(2-bromo)acetyl]amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propane was obtained in quantitative yield. No further purification was necessary.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05684033
出典データセットuspto-grants-1997_11
ORD IDord-59a3b528a97d44cfbe0327e652d13540
出典メモuspto-grants-1997_11