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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356855Generated: October 30, 2026

3-Amino-4-(1H-indol-3-yl)butanoic acid--hydrogen chloride (1/1) → (S)-3-(1H-Indol-3-ylmethyl)-1-(2-phenyl-ethyl)-2-oxo-piperazine

https://huagongshe.com/reaction/356855

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-4-(1H-indol-3-yl)butanoic acid--hydrogen chloride (1/1)HCID 2761549—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantN-t-butoxycarbonyl-N-(2-oxo-ethyl)-2-phenyl-ethylamineHCID 23225807—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(S)-3-(1H-Indol-3-ylmethyl)-1-(2-phenyl-ethyl)-2-oxo-piperazineHCID 9905691—

Reaction Steps

Combine N-t-butoxycarbonyl-N-(2-oxo-ethyl)-2-phenyl-ethylamine (5.10 g, 19.16 mmol) and (S)-2-(1H-indol-3-yl)-1-carboxymethyl-ethylamine hydrochloride salt ((S)-tryptophan methyl ester hydrochloride salt) (4.90 g, 19.23 mmol) in methanol (50 mL) and stir for 10 minutes. Add sodium cyanoborohydride in solution (19.0 mL, 1M in THF, 19.0 mmol) and stir under an inert atmosphere for 18 hours. Concentrate in vacuo to obtain a residue. Dilute the residue with ethyl acetate and extract with water. Separate the layers, dry the organic layer over MgSO4, filter, and evaporate in vacuo. Chromatograph on silica gel eluting with 50% ethyl acetate/hexane to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840726
Source datasetuspto-grants-1998_11
ORD IDord-aacedfdc36db4acfbcbf8e5fcad0acd4
Source noteuspto-grants-1998_11