돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1242538생성일: 2026년 10월 27일

Lysergic Acid → Lysergic Acid N-ethyl N-(2-carbethoxy)ethyl Amide

https://huagongshe.com/reaction/1242538

반응식

참여 물질

역할이름HCID투입량
반응물Lysergic AcidHCID 6717—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물Ethyl N-ethyl-beta-alaninateHCID 90223—
용매DimethylformamideHCID 6228—
생성물Lysergic Acid N-ethyl N-(2-carbethoxy)ethyl AmideHCID 66871214—

반응 단계

A mixture of lysergic acid 5 (934 mg, 3.27 mmol) in 40 ml of dry dimethylformamide (DMF) was treated with 1,1′-carbonydidimidazole (CDI, 795 mg, 4.91 mmol) and stirred under nitrogen at room temperature for 1 hour. The N-ethyl N-(2-carbethoxy)ethyl amine linker 10 (1.90 g, 13.08 mmol) in 10 ml of dry dimethylformamide (DMF) was added dropwise and the reaction solution was stirred overnight at room temperature. The reaction solution was concentrated under reduced pressure and the resulting residue was dissolved in 200 ml of chloroform. The chloroform solution was washed twice with 100 ml of water, dried over anhydrous sodium sulphate, and concentrated under reduced pressure to yield the crude title compound 6 (2.2 g) as an oil. This was used without further purification in the following Example. υmax/cm−1 3121.90, 2987.10, 2848.65, 1735.30, 1676.97, 1202.97 (FT-IR: FIG. 9)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07115718B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-9fe6948392e045f8a8eb03a20c72f160
출처 메모uspto-grants-2006_10