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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872491Generated: October 30, 2026

Tris(hydroxymethyl)aminomethane → N-(2-(3-(3-chloro-4-cyanophenyl)-1H-pyrazol-1-yl)ethyl)-5-(1-methyl-1H-pyrazol-4-yl)isoxazole-3-carboxamide

https://huagongshe.com/reaction/872491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(hydroxymethyl)aminomethaneHCID 6503—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantCarbodiimideHCID 160435—
Reactant5-(1-methyl-1H-pyrazol-4-yl)-1,2-oxazole-3-carboxylic acidHCID 3161122—
Reactant4-(1-(2-Aminoethyl)-1H-pyrazol-3-yl)-2-chlorobenzonitrileHCID 67170166—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN-(2-(3-(3-chloro-4-cyanophenyl)-1H-pyrazol-1-yl)ethyl)-5-(1-methyl-1H-pyrazol-4-yl)isoxazole-3-carboxamideHCID 5291982719%

Reaction Steps

5-(1-methyl-1H-pyrazol-4-yl)isoxazole-3-carboxylic acid (57.9 mg, 0.3 mmol), HOBt (46 mg, 0.340 mmol) and PS-carbodiimide (364 mg), DCM (4 ml) and DMF (0.4 ml) were mixed in a glass vial. The mixture was shaken for 10 min. 4-(1-(2-aminoethyl)-1H-pyrazol-3-yl)-2-chlorobenzonitrile (49 mg, 0.20 mmol) was added and the mixture was stirred for 24 h. The solids were filtered off. PS-Trisamine (333 mg, 1.0 mmol) was added to the filtrate. The mixture was shaken for 4 h and filtered. The filtrate was concentrated and purified by flash chromatography (gradient of DCM:MeOH) to give 16 mg of the title compound. 1H-NMR (400 MHz; d6-DMSO): 3.70 δ (m, 2H), 3.91 (s, 3H), 4.38 (m, 2H), 6.89 (m, 1H), 6.97 (d, 1H), 7.85 (m, 1H), 7.94-8.00 (m, 3H), 8.10 (d, 1H), 8.36 (s, 1H), 8.86-9.13 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975254B2
Source datasetuspto-grants-2015_03
ORD IDord-c2cf3499b9a64eac8fb98556906e85e7
Source noteuspto-grants-2015_03