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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2201109생성일: 2026년 10월 24일

tert-Butyl (1R)-2-amino-1-(1H-indol-3-ylmethyl)-2-oxoethylcarbamate → D-tryptophanamide

https://huagongshe.com/ko/reaction/2201109

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl (1R)-2-amino-1-(1H-indol-3-ylmethyl)-2-oxoethylcarbamateHCID 57107549—
용매Hydrochloric AcidHCID 313—
용매1,4-DioxaneHCID 31275—
생성물D-tryptophanamideHCID 688582—

반응 단계

A solution of (R)-tert-butyl 1-amino-3-(1H-indol-3-yl)-1-oxopropan-2-ylcarbamate (0.963 g, 3.18 mmol) in 4N HCl in dioxane (8 mL) was stirred at room temperature for 1 h. It was then concentrated in vacuo. The residue was partitioned between nBuOH and aq. 5% NaHCO3. The nBuOH phase was separated, washed with water, concentrated in vacuo to give (R)-2-amino-3-(1H-indol-3-yl)propanamide as free base (0.324 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09359375B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-d5cc52ab9ea44a97af10290ad8d4ef7a
출처 메모uspto-grants-2016_06