Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009891Generated: October 30, 2026

Tris(hydroxymethyl)aminomethane → HCID 67304415, compound

https://huagongshe.com/reaction/1009891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(hydroxymethyl)aminomethaneHCID 6503—
Reactant4-MethylmorpholineHCID 7972—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 67303976HCID 67303976—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 67304415HCID 6730441535%

Reaction Steps

To a chloroform solution (300 μL) of 1,1′-carbonyldiimidazole (7.30 mg, 0.045 mmol) were added a chloroform solution (150 μL) of (1S)-1-[5-[4-(2-aminoethyl)benzyl]-2-acetoxy-4-methylphenyl]-1,5-anhydro-2,3,4,6-tetra-O-acetyl-D-glucitol (18.4 mg, 0.030 mmol) and N-methyl morpholine (4.95 μL, 0.045 mmol), and the mixture was stirred for 30 minutes at room temperature. After that, to this reaction solution were added tris(hydroxymethyl)aminomethane (10.9 mg, 0.09 mmol) and N,N-dimethylformamide (150 μL), and this reaction mixture was stirred at 60° C. overnight. After the reaction mixture was cooled to room temperature, ethyl acetate was added thereto. And the mixture was washed with water, 1 M hydrochloric acid, and brine, and dried with anhydrous magnesium sulfate. The drying agent was filtered off, and the solvent was evaporated under reduced pressure. Thus obtained residue was purified with silica gel column chromatography (chloroform:methanol=95:5) to obtain the title compound (7.9 mg, 35%) as a colorless amorphous compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973012B2
Source datasetuspto-grants-2011_07
ORD IDord-56caeeacece84161920f8ee6859b240a
Source noteuspto-grants-2011_07