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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108570Generated: October 27, 2026

Cyclooctylamine → n-Cyclooctyl-5-phenyl-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxamide

https://huagongshe.com/reaction/2108570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclooctylamineHCID 2903—
ReactantDimethylformamideHCID 6228—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant4,4,4-Trifluoro-1-phenyl-1,3-butanedioneHCID 67589—
Reactant1-HydroxybenzotriazoleHCID 75771—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Productn-Cyclooctyl-5-phenyl-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxamideHCID 13607121096%

Reaction Steps

Cyclooctylamine (24 mg, 0.19 mmol) was added to a suspension of compound 1 (0.05 g, 0.16 mmol), WSC (37 mg, 0.19 mmol), HOBt (29 mg, 0.19 mmol) and DMAP (23 mg, 0.19 mmol) in DMF (1.5 mL). The reaction mixture was stirred at room temperature for 14 h, diluted with DCM (0.5 mL) and saturated NaHCO3 solution (0.5 mL), and then separated using PHASE-SEP filtration syringe. The organic layer was concentrated and loaded onto preparative HPLC (Gilson 215 system). The purest fractions were combined to give 64.6 mg (96% yield) of the title compound as a white solid. Reverse Phase LC/MS: CAPCELLPAKCC18UG120, S-3 μm, 2.0×50 mm, UV detection at 220, 8 min. gradient 10-100% Solvent B/A (Solvent A: CH3CN with 0.1% TFA, Solvent B: H2O with 0.1% TFA), 0.5 mL/min. Rt=1.90 min, (96% pure). MS (M+H: 421).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514441B2
Source datasetuspto-grants-2009_04
ORD IDord-5e3e14dfbf664f1ebb2b057a179f21cc
Source noteuspto-grants-2009_04