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HRID 1379049作成日:2026年10月25日

Formic Acid → 2-amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propane

https://huagongshe.com/reaction/1379049

反応式

関与物質

役割名称HCID仕込み量
反応物Formic AcidHCID 284—
反応物3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]-2-(N-triphenylmethylamino)propaneHCID 22508951—
溶媒DichloromethaneHCID 6344—
生成物2-amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propaneHCID 2250895590%

反応手順

Formic acid (9.0 ml, 238.540 mmoles) was added to a stirring solution of 3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]-2-(N-triphenylmethylamino)propane (14.11 g, 23.763 mmoles) in anhydrous methylene chloride under a nitrogen atmosphere at 0° C. After 4 hours, the reaction mixture was concentrated to an oil on a rotary evaporator and redissolved in diethyl ether and 1.0N hydrochloric acid. The aqueous layer was washed twice with diethyl ether and basified with sodium hydroxide to a pH greater than 12. The product was extracted out with methylene chloride (4×). The organic extracts were combined, dried over anhydrous sodium sulfate, filtered, and concentrated on a rotary evaporator to a white foam. The compound 2-amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propane (7.52 g, 21.397 mmols) was isolated giving a 90% yield. No further purification was necessary.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05670499
出典データセットuspto-grants-1997_09
ORD IDord-c3a4d9a84e5d425db79d1d61f7826400
出典メモuspto-grants-1997_09