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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260361Generated: November 3, 2026

Diisopropylethylamine → HCID 87464014, compound

https://huagongshe.com/reaction/1260361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(3S)-pyrrolidin-3-olHCID 2733874—
ReactantHCID 87462668HCID 87462668—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 87464014HCID 87464014—

Reaction Steps

A solution of (Z)-3-methyl-1-(5-methyl-3-(2,2,3,3-tetrafluoro-2,3-dihydrobenzo[b][1,4]dioxin-6-yl)thiazol-2(3H)-ylidenecarbamoyl)-1H-imidazol-3-ium iodide (Example 81A, 0.1 g, 0.18 mmol), (S)-pyrrolidin-3-ol (0.016 g, 0.18 mmol) and Hunig's base (0.023 g, 018 mmol) in dry acetonitrile (5 mL) was heated to 60° C. for three hours. After cooling, the mixture was diluted with CH2Cl2 (50 mL) and washed with water and brine. The organic phase was dried over sodium sulfate, filtered and dried. After evaporation under reduced pressure, the residue was chromatographed over silica using CH2Cl2 and then 2% MeOH/CH2Cl2 to give the titled compound. 1H NMR (CDCl3) δ ppm 1.99 (2 H), 2.20 (3 H), 3.40-3.70 (4 H), 4.42 (1 H), 6.60 (1 H), 7.20-7.50 (3 H); MS (ESI) m/z 434(M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470813B2
Source datasetuspto-grants-2013_06
ORD IDord-2930cde6d2014f978e1113822717eee5
Source noteuspto-grants-2013_06