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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356852Generated: October 30, 2026

Sodium cyanoborohydride → (R)-3-(1H-Indol-3-ylmethyl)-1-(2-phenyl-ethyl)-2-oxo-piperazine

https://huagongshe.com/reaction/356852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantN-t-butoxycarbonyl-N-(2-oxo-ethyl)-2-phenyl-ethylamineHCID 23225807—
Reactant(R)-3-Amino-4-(1H-indol-3-yl)butanoic acid hydrochlorideHCID 51064127—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(R)-3-(1H-Indol-3-ylmethyl)-1-(2-phenyl-ethyl)-2-oxo-piperazineHCID 15391969—

Reaction Steps

Combine N-t-butoxycarbonyl-N-(2-oxo-ethyl)-2-phenyl-ethylamine (5.03 g, 19.0 mmol) and (R)-2-(1H-indol-3-yl)-1-carboxymethyl-ethylamine hydrochloride salt ((R)-tryptophan methyl ester hydrochloride salt) (4.9 g, 19.42 mmol) in methanol (50 mL) and stir for 30 minutes. Add sodium cyanoborohydride in solution (15.0 mL, 1M in THF, 15.0 mmol) and stir under an inert atmosphere for 16.5 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-a80987f40a714dab88f60e6e8ed1c04e
Source noteuspto-grants-1998_11