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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1379049생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1379049

반응식

참여 물질

역할이름HCID투입량
반응물Formic AcidHCID 284—
반응물3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]-2-(N-triphenylmethylamino)propaneHCID 22508951—
용매DichloromethaneHCID 6344—
생성물2-amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propaneHCID 2250895590%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05670499
출처 데이터셋uspto-grants-1997_09
ORD IDord-c3a4d9a84e5d425db79d1d61f7826400
출처 메모uspto-grants-1997_09