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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394454Generated: November 3, 2026

Trifluoroacetic acid → HCID 178493715, compound

https://huagongshe.com/reaction/1394454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantBis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
ReactantN,N-Diethyl-2-propanamineHCID 521913—
Reactant4-[1-Phenyl-1-(5-methyl-1,3,4-oxadiazol-2-yl)methylene]-piperidine-1-carboxylic acid tert-butyl esterHCID 67046471—
ReactantHCID 178493717HCID 178493717—
SolventDichloromethaneHCID 6344—
ProductHCID 178493715HCID 17849371518%

Reaction Steps

To a solution of 4-[1-phenyl-1-(5-methyl-1,3,4-oxadiazol-2-yl)methylene]-piperidine-1-carboxylic acid tert-butyl ester (0.0348 g, 0.098 mmol) in CH2Cl2 (1 mL) was added TFA (0.5 mL) and the reaction mixture was stirred for 30 min. The solvent was then removed in vacuo and the residual material was dissolved in CHCl3 (1 mL). To this solution was then added 4-methoxy-7-(5-methyl-1,3,4-triazol-2-yl)-6-azaindol-3-yl-oxoacetic acid hydrochloride salt (0.0621 g, 0.206 mmol) and iPrNEt2 (0.18 mL, 1.03 mmol), followed by BOP—Cl (0.0670 g, 0.263 mmol). The mixture was stirred at rt for 2 h and then the solvent was removed in vacuo. The residue was diluted with H2O and extracted with EtOAc (×3). The combined organic layers were washed (H2O, brine), dried (Na2SO4) and concentrated, and the residue was purified by preparative HPLC (NH4OAc) to give the title compound (0.0093 g, 18%) as a colorless solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348337B2
Source datasetuspto-grants-2008_03
ORD IDord-0ae2a2633ae04ccf9a872c28f7ffb29e
Source noteuspto-grants-2008_03