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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245380Generated: October 31, 2026

Acetonitrile → (NZ)-N-[5-methylidene-3-(2,2,3,3-tetrafluoro-1,4-benzodioxin-6-yl)-1,3-thiazolidin-2-ylidene]imidazole-1-carboxamide

https://huagongshe.com/reaction/2245380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantDiisopropylethylamineHCID 81531—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Reactant5-Methylene-3-(2,2,3,3-tetrafluoro-2,3-dihydrobenzo[b][1,4]dioxin-6-yl)thiazolidin-2-imineHCID 86619167—
Product(NZ)-N-[5-methylidene-3-(2,2,3,3-tetrafluoro-1,4-benzodioxin-6-yl)-1,3-thiazolidin-2-ylidene]imidazole-1-carboxamideHCID 87463827—

Reaction Conditions

Temperature80 °C

Reaction Steps

The crude imine (Example 22C, 169 mg, <0.52 mmol) was dissolved into acetonitrile (10 mL), treated with diisopropylethylamine (130 μL, 0.75 mmol) and carbonyl diimidazole (94 mg, 0.58 mmol), and then heated near 80° C. overnight. The mixture was concentrated and chromatographed through silica (10/40/50 to 25/25/50% EtOAc/CH2Cl2/hexanes) to give the titled compound. 1H NMR (300 MHz, CDCl3) δ ppm 4.83 (2H), 5.42 (1H), 5.45 (1H), 7.01 (1H), 7.26-7.35 (3H), 7.44 (1H), 8.10 (1H); MS (ESI) m/z 415 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683084B2
Source datasetuspto-grants-2010_03
ORD IDord-706b0a8a95eb4a3a9724eadd6dfc852f
Source noteuspto-grants-2010_03