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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034998Generated: November 2, 2026

Trifluoroacetic acid → HCID 68582561, compound

https://huagongshe.com/reaction/1034998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Cyano-2-fluoropyridineHCID 2783254—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68582561HCID 6858256151%

Reaction Conditions

Temperature115 °C

Reaction Steps

The product from Example 88B (1.57 g, 7.9 mmol) in dichloromethane (25 mL) was treated with trifluoroacetic acid (5 mL) for 30 min at rt. The reaction mixture was concentrated to dryness. To the residue was added 2-fluoro-nicotinonitrile (1.0 g, 8.19 mmol) and diisopropyl ethylamine (3.2 mL) in tetrahydrofuran (8 mL). The reaction mixture was heated at 115° C. for 10 min under microwave condition. The mixture was concentrated to dryness, and the residue was chromatographed using hexane/ethyl acetate (9:1-6:1) to give the title compound (806 mg, 51%). MS (DCI/NH3) m/z 202 (M+1)+. 1HNMR (400 MHz, CDCl3) δ ppm 1.98 (s, 2 H) 3.67 (d, J=10.13 Hz, 1 H) 3.91 (dd, J=7.98, 1.53 Hz, 1 H) 3.96 (m, 2 H) 4.69 (s, 1 H) 5.16 (s, 1 H) 6.64 (dd, J=7.67, 4.91 Hz, 1 H) 7.71 (dd, J=7.36, 1.84 Hz, 1 H) 8.26 (dd, J=4.60, 1.84 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546374B2
Source datasetuspto-grants-2013_10
ORD IDord-6a272794a6854cad8c35718ddafb9a4a
Source noteuspto-grants-2013_10