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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626781Generated: October 25, 2026

Triethylamine → HCID 178510122, compound

https://huagongshe.com/reaction/626781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Amino-3-chloro-5-fluorobenzonitrileHCID 66801728—
Reactant4-Azido-5-fluoropyridine-3-carbaldehydeHCID 86697053—
CatalystTitanium TetrachlorideHCID 24193—
SolventDichloromethaneHCID 6344—
ProductHCID 178510122HCID 17851012289%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4-azido-5-fluoro-3-pyridinecarboxaldehyde (1.0 g, 6.02 mmol) and 2-amino-3-chloro-5-fluorobenzonitrile (1.03 g, 6.02 mmol) in anhydrous DCM (20 mL) was cooled in an icebath and triethylamine (2.52 mL, 18.07 mmol) was added, followed by titanium (IV) chloride (1 N in DCM, 3.6 mL, 3.6 mmol). The reaction mixture was stirred at 0° C. for 3 hours and then at room temperature overnight. The resultant mixture was concentrated under reduced pressure and the residue was suspended in ethyl acetate and filtered through a pad of Celite®. The filtrate was concentrated under reduced pressure to afford the title compound as a pale brown solid (1.67 g, 89% yield), which was used directly in the next step without purification. LCMS (Method C): RT=3.74 min, m/z: 291 [M+H+−N2].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309240B2
Source datasetuspto-grants-2016_04
ORD IDord-200e3b0b2c2e43eb858db134238757f6
Source noteuspto-grants-2016_04