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HRID 84877作成日:2026年10月25日

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

https://huagongshe.com/reaction/84877

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl (1R)-2-amino-1-(1H-indol-3-ylmethyl)-2-oxoethylcarbamateHCID 57107549—
溶媒Hydrochloric AcidHCID 313—
溶媒1,4-DioxaneHCID 31275—
生成物D-tryptophanamideHCID 688582—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846928B2
出典データセットuspto-grants-2014_09
ORD IDord-6397bec98d2d4881903b1d6ae08634cb
出典メモuspto-grants-2014_09