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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214647Generated: October 30, 2026

Trifluoroacetic acid → HCID 54704658, compound

https://huagongshe.com/reaction/2214647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-(4-Pyridyl)piperazineHCID 70517—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 54704627HCID 54704627—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductHCID 54704658HCID 5470465812%

Reaction Steps

A solution of 1-(2,2-dimethoxy-ethyl)-4-hydroxy-5-oxo-2,5-dihydro-1H-pyrrole-3-carboxylic acid (3,4-dichloro-benzyl)-methyl-amide (0.29 g, 0.71 mmol) in acetonitrile/water (10 mL, 2.5:1) was stirred with trifluoroacetic acid (1 mL) overnight at room temp. The mixture was concentrated then dissolved in MeOH (3 mL). 1-(4-pyridyl)-piperazine (0.42 g, 2.6 mmol) was added and the resulting mixture was stirred at room temp 30 min. Sodium cyanoborohydride (0.013 g, 0.2 mmol) was added and the mixture was stirred an additional 5 h at room temp. The crude product was purified by preparative HPLC (YMC Combiprep ODS-A, 30 mm×50 mm, MeOH/H2O/0.1% TFA) to yield the title compound as an amber foam (0.0042 g, 12% yield). HRMS (M+H) calcd for C24H28N5Cl2O3: 504.15693; found: 504.1564.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109186B2
Source datasetuspto-grants-2006_09
ORD IDord-9250a01aac7f468f9e57123b43c7905b
Source noteuspto-grants-2006_09