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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7272생성일: 2026년 10월 24일

L-Methionine → tert-Butyl N-[(benzyloxy)carbonyl]-L-methionyl-L-alaninate

https://huagongshe.com/ko/reaction/7272

반응식

참여 물질

역할이름HCID투입량
반응물L-MethionineHCID 6137—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물L-Alanine 1,1-dimethylethyl esterHCID 89016—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
생성물tert-Butyl N-[(benzyloxy)carbonyl]-L-methionyl-L-alaninateHCID 16124765109.3%

반응 단계

Z-Protected L-methionine (10 g) was dissolved in DMF (200 ml) and 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (8.13 g) was added followed by HOBT (5.72 g) and triethylamine (19.7 ml). The mixture was stirred for 1 h then L-alanine tert-butyl ester (7.7 g) was added and stirring continued for 18 h. The mixture was concentrated under reduced pressure and partitioned between diethyl ether and water. The separated organic phase was washed with hydrochloric acid (1M), saturated sodium bicarbonate solution and brine, dried (over magnesium sulphate) and concentrated under reduced pressure to give the title compound (11.9 g) as an orange oil which crystallised on standing.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084139B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-acb43fa5eb1b42d09e33b5d59c24f091
출처 메모uspto-grants-2006_08