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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26035생성일: 2026년 10월 24일

Triethylamine → 5-Amino-2,10-dimethyl-4,8-dioxo-5-vinyl-3,9-diazaundecanedioic acid

https://huagongshe.com/ko/reaction/26035

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물L-Alanine methyl esterHCID 82335—
반응물2-(Benzyloxycarbonyl)amino-2-vinylglutaric acidHCID 21326441—
용매DichloromethaneHCID 6344—
생성물5-Amino-2,10-dimethyl-4,8-dioxo-5-vinyl-3,9-diazaundecanedioic acidHCID 21326422—

반응 조건

온도25 °C

반응 단계

To 2-(benzyloxycarbonyl)amino-2-vinylglutaric acid (305 mg, 1 mM) in methylene chloride (15 ml) is added triethylamine (205 mg, 2 mM) followed by ethyl chloroformate (218 mg, 2 mM). The solution is stirred for one hour at 25° C., then alanine methyl ester (206 mg, 2 mM) in methylene chloride (5 ml) is added. This solution is kept overnight at 25° C., washed with water, dried and evaporated to dryness. The residue is treated with 5 ml of a 40% (w/w) solution of hydrogen bromide in dioxane at 25° C. for 30 minutes. Ether (50 ml) is then added and the precipitate collected. This is then treated with 20 ml of a 1 N sodium hydroxide solution overnight at 25° C., the pH adjusted to 6.5, and applied to an Amberlite 120 H+ resin. Elution with 2 N ammonium hydroxide afforded 5-amino-2,10-dimethyl-4,8-dioxo-5-vinyl-3,9-diazaundecanedioic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04147873
출처 데이터셋uspto-grants-1979_04
ORD IDord-dbca350db4ff403ca0a0c18ad91427fb
출처 메모uspto-grants-1979_04