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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874635Generated: October 28, 2026

Diisopropylethylamine → N-(5-(2,2-difluoro-6-methylbenzo[d][1,3]dioxol-5-yl)pyrazin-2-yl)-2,6-difluorobenzamide

https://huagongshe.com/reaction/874635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2,6-Difluorobenzoyl chlorideHCID 87438—
ReactantHCID 58487049HCID 58487049—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
ProductN-(5-(2,2-difluoro-6-methylbenzo[d][1,3]dioxol-5-yl)pyrazin-2-yl)-2,6-difluorobenzamideHCID 5848708465.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

Under an atmosphere of argon, 2,6-difluorobenzoyl chloride (40 mg, 0.2 mmol) was added to a stirred solution of 9 (30 mg, 0.1 mmol) and Hünig's base (120 μL, 88 mg, 0.7 mmol) in dichloromethane (1.0 mL) at room temperature. The reaction was stirred for 0.5 h. The solution was diluted with tetrahydrofuran (0.9 mL), methanol (0.6 mL) and 2 M sodium hydroxide solution (0.2 mL). The mixture was stirred and heated to 60° C. for 10 min then cooled to room temperature, extracted with dichloromethane (3×5 mL), dried with sodium sulfate and concentrated under reduced pressure. Flash chromatography (ISCO system, silica, 0-20% ethyl acetate in hexane) provided 10 (26.4 mg, 58%) as a crystalline solid: LRESIMS m/z 406.1 [M+H]+, calcd. for C19H12F4N3O3 406.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980629B2
Source datasetuspto-grants-2015_03
ORD IDord-d798c3e934fe4bc3a7768a5c04a0ff88
Source noteuspto-grants-2015_03