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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499210Generated: October 25, 2026

Tris(hydroxymethyl)aminomethane → HCID 59420891, compound

https://huagongshe.com/reaction/499210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(hydroxymethyl)aminomethaneHCID 6503—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-((Pyridin-4-yl)methyl)piperazineHCID 808715—
ReactantHCID 59420892HCID 59420892—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 59420891HCID 59420891—

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of 4-[3-(5-tert-butyl-2-methyl-2H-pyrazol-3-yl)-ureido]benzoic acid (0.08 g, 0.26 mmol) in a mixture of dichloromethane (4 mL) and DMF (0.20 mL) is added 1-(4-pyridinylmethyl)piperazine (0.046 g, 0.26 mmol), PS-DCC (0.41 g, 0.52 mmol) and HOBT (0.035 g, 0.26 mmol). The mixture is stirred overnight at 45° C. in a closed tube (orbital stirring). Then PS-Trisamine is added (0.52 mmol) and the mixture is stirred for 4 hr at room temperature, filtrated, and washed three times with dichloromethane. The solvents are evaporated under reduced pressure and the residue is purified by biotage column chromatography (eluent: ethyl acetate/methanol 10:1) to give 0.020 g (0.04 mmol), 16% as white solid. ES+(m/z)=476 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767674B2
Source datasetuspto-grants-2010_08
ORD IDord-813e2fcf51114c428f7ac57a1c0ba47b
Source noteuspto-grants-2010_08