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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402633Generated: October 30, 2026

3-Methylenecyclobutanecarboxylic acid → N-((3-chloropyrazin-2-yl)methyl)-3-methylenecyclobutanecarboxamide

https://huagongshe.com/reaction/2402633

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methylenecyclobutanecarboxylic acidHCID 27475—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantDiisopropylethylamineHCID 81531—
Reactant(3-Chloropyrazin-2-yl)methanamine dihydrochlorideHCID 42609650—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductN-((3-chloropyrazin-2-yl)methyl)-3-methylenecyclobutanecarboxamideHCID 57681076—

Reaction Conditions

Temperature60 °C

Reaction Steps

1,1′-Carbonyldiimidazole (CDI) (8.24 g, 50.81 mmol) and 3-methylenecyclobutanecarboxylic acid (5.70 g, 50.81 mmol) were dissolved in anhydrous THF (100 mL) and allowed to stir at 60° C. for 4 h. A solution of C-(3-Chloropyrazin-2-yl)methylamine bis-hydrochloride (10.0 g, 46.19 mmol) and diisopropylethylamine (DIPEA) (32.30 mL, 184.76 mmol) in anhydrous CH2Cl2 (150 mL) was added to the mixture and the reaction was allowed to stir at rt for 24 h. The mixture was concentrated in vacuo, the residue dissolved in EtOAc and the resulting solution washed with saturated NaHCO3 (aq.) water HO and Brine. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to afford crude product, which was purified by chromatography over silica gel eluting with 50-70% EtOAc/hexane to yield desired product. 1H NMR (400 MHz, CDCl3) δ ppm 2.92-2.94 (2H, m), 3.05-3.14 (2H, m), 4.60 (2H, d, J=4.24 Hz), 4.80-4.84 (2H, m), 6.75 (1H, brs), 8.33 (1H, d, J=4.22 Hz) and 8.45 (1H, d, J=2.54 Hz). MS (ES+): m/z 238 and 240 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796455B2
Source datasetuspto-grants-2014_08
ORD IDord-d361d7510b1a41a28114c6fd4dbef0fa
Source noteuspto-grants-2014_08