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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926872Generated: October 24, 2026

Diisopropylethylamine → HCID 66587597, compound

https://huagongshe.com/en/reaction/926872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-3-amineHCID 13626946—
Reactant2-Nitro-5-(piperidin-1-yl)benzoic acidHCID 14459331—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 66587597HCID 6658759736.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

Into a 250-mL round bottom flask, was placed a solution of 2-nitro-5-(piperidin-1-yl)benzoic acid (5 g, 20.00 mmol, 1.19 equiv) in N,N-dimethylformamide (50 mL), 1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-3-amine (3.8 g, 16.74 mmol, 1.00 equiv), HATU (9.5 g, 25.00 mmol, 1.49 equiv), and N,N-diisopropylethylamine (3.3 g, 25.58 mmol, 1.53 equiv). The resulting solution was stirred overnight at 50° C. in an oil bath. The reaction progress was monitored by LCMS. The resulting solution was diluted with 200 mL of water, extracted with 4×50 mL of ethyl acetate, and the organic layers combined. The resulting mixture was washed with 2×50 mL of water and 2×50 mL of brine. The mixture was dried over sodium sulfate. The solids were filtered out. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column and eluted with petroleum ether/ethyl acetate (5:1) to yield 2.8 g (36%) of product as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09289430B2
Source datasetuspto-grants-2016_03
ORD IDord-15e29229d098487dbe70c98bd9b953b5
Source noteuspto-grants-2016_03