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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201109Generated: October 26, 2026

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

https://huagongshe.com/reaction/2201109

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (1R)-2-amino-1-(1H-indol-3-ylmethyl)-2-oxoethylcarbamateHCID 57107549—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
ProductD-tryptophanamideHCID 688582—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359375B2
Source datasetuspto-grants-2016_06
ORD IDord-d5cc52ab9ea44a97af10290ad8d4ef7a
Source noteuspto-grants-2016_06