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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270801Generated: October 30, 2026

Triethylamine → HCID 21071120, compound

https://huagongshe.com/reaction/270801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(4-Chlorophenyl)piperazineHCID 97478—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant5-(Azidomethyl)-4-chloro-3-(trifluoromethyl)-1H-pyrazole-1-acetic acidHCID 21071157—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 21071120HCID 21071120—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 2.71 g (13.7 mmol) of 1-(4-Chlorophenyl)piperazine and 3.58 g (12.5 mmol) of (5-Azidomethyl-4-chloro-3-trifluoromethyl-pyrazol-1-yl)-acetic acid in 40 mL of anhydrous dimethylformamide was added 4.36 mL (31.2 mmol) of triethylamine. The solution was cooled to 0° C., and 5.21 g (13.7 mmol) of O-(7-Azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HATU) was added. After 2 hours the reaction was diluted with two volumes of water, and the solvent was decanted away from the resulting oil. The oil was crystallized by dissolving in methanol and adding water in small portions. The product was isolated as a white solid by filtration: 1H NMR (DMSO-d6, 400 MHz) 7.23 (d, 2H), 6.97 (d, 2H), 5.48 (s, 2H), 4.62 (s, 2H), 3.60 (m, 4H), 3.24 (m, 2H), 3.12 (m, 2H) ppm; MS (ES) M+H expected=462.1, found=462.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449576B1
Source datasetuspto-grants-2008_11
ORD IDord-fc7b403daf014c7ead8ca555d00c1765
Source noteuspto-grants-2008_11