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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563147Generated: October 29, 2026

Water → HCID 59808274, compound

https://huagongshe.com/reaction/563147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIndole-5-carboxaldehydeHCID 589040—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 10687394HCID 10687394—
SolventMethanolHCID 887—
ProductHCID 59808274HCID 5980827488.4%

Reaction Steps

In an inert atmosphere, indole-5-carboxaldehyde (108 mg, 0.75 mmol) and 2-amino-1-(4-benzyl-piperazin-1-yl)-(S)-3-phenyl-propan-1-one (162 mg, 0.50 mmol) were dissolved in dry MeOH (4.0 mL) and refluxed for 4 h. The reaction mixture was cooled to rt followed by slow addition of sodium borohydride (28 mg, 0.75 mmol). Stirring was continued for 1 h. Water (1 mL) was added to the reaction mixture followed by evaporation of the solvent under reduced pressure. The residue was dissolved in EtOAc (10 mL) and washed with sat. sodium hydrogencarbonate solution (10 mL) and brine (10 mL). The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo to give 200 mg (80%) of 1-(4-benzyl-piperazin-1-yl)-2-[(1H-indol-5-ylmethyl)-amino]-(S)-3-phenyl-propan-1-one. LC-MS: tR=0.65 min; [M+H]+=453.39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067419B2
Source datasetuspto-grants-2011_11
ORD IDord-2fc73d96caff41a3b6fcc150f0cfb168
Source noteuspto-grants-2011_11