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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466184Generated: November 4, 2026

2,6-Diaminopyridine → HCID 178507624, compound

https://huagongshe.com/reaction/1466184

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DiaminopyridineHCID 8861—
ReactantHCID 86710863HCID 86710863—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 178507624HCID 17850762455.3%

Reaction Steps

A solution of 4-(trifluoromethyl)-N-((2-(trifluoromethyl)benzyl)carbamothioyl) benzamide (2.0 g, 4.92 mmol), 2,6-diaminopyridine (591 mg, 5.41 mmol), and 1-ethyl-3-(3-dimethyllaminopropyl)carbodiimide hydrochloride (EDC hydrochloride) (1.13 g, 5.91 mmol) in DMF (49 mL) was heated to 65° C. for 30 minutes, then allowed to cool to room temperature. The mixture was then diluted with ethyl acetate, washed with aqueous sodium bicarbonate solution, washed with brine, dried over sodium sulfate, and concentrated to provide the crude product. The crude product was purified by chromatography (gradient: 9:1 hexanes:EtOAc to 6:4 hexanes:EtOAc) to provide (Z)—N-(((6-aminopyridin-2-yl)amino)((2-(trifluoromethyl) benzyl)amino)methylene)-4-(trifluoromethyl)benzamide as a yellow solid (1.31 g, 55% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000014B2
Source datasetuspto-grants-2015_04
ORD IDord-07d5e2f33ab94c3c97d804523ffcbbb4
Source noteuspto-grants-2015_04