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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238375Generated: October 30, 2026

N'-Hydroxy-4-(trifluoromethyl)benzene-1-carboximidamide → HCID 86684874, compound

https://huagongshe.com/reaction/238375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN'-Hydroxy-4-(trifluoromethyl)benzene-1-carboximidamideHCID 609329—
Reactant1-methyl-1H-pyrazole-5-carboxylic acidHCID 643158—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86684874HCID 8668487429.8%

Reaction Steps

N′-hydroxy-4-(trifluoromethyl)benzene carboximidamide (450 mg) was added to a tetrahydrofuran (8.8 mL) suspension that contained 1-methyl-1H-pyrazol-5-carboxylic acid (450 mg), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (465 mg) and 1-hydroxybenzotriazole monohydrate (328 mg) at a room temperature, and the obtained solution was then stirred for 16 hours. Thereafter, potassium tert-butoxide (1.11 g) and tetrahydrofuran (4.4 mL) were added to the reaction solution, and the obtained mixture was then stirred at a room temperature for 3 hours. Thereafter, water was added to the reaction solution, and the obtained mixture was then extracted with ethyl acetate. The organic layer was washed with a saturated saline, and was then dried over anhydrous magnesium sulfate, followed by vacuum concentration. The residue was purified by column chromatography (silica gel cartridge, hexane:ethyl acetate=75:25 to 50:50), so as to obtain the title compound (193 mg) in the form of a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642626B2
Source datasetuspto-grants-2014_02
ORD IDord-ce571f2915bd4303891d1f4cd029e9f4
Source noteuspto-grants-2014_02