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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493758Generated: October 26, 2026

Phosphorus oxychloride → 7-(8-Chloro-3-cyclobutylimidazo[1,5-a]pyrazin-1-yl)-quinoline

https://huagongshe.com/reaction/493758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN-[(3-chloro-2-pyrazinyl)-7-quinolinylmethyl]cyclobutanecarboxamideHCID 57680974—
Product7-(8-Chloro-3-cyclobutylimidazo[1,5-a]pyrazin-1-yl)-quinolineHCID 57680887—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of POCl3 (8 mL, 13 g, 87 mmol) and cyclobutanecarboxylic acid [(3-chloropyrazin-2-yl)-quinolin-7-ylmethyl]-amide (566 mg, 1.60 mmol) was heated to 55° C. for 21.5 h and to 70° C. for 6 h. POCl3 was evaporated, a cold solution of NH3 in iPrOH (2 M, 10 mL) was added, the suspension was filtered, and the solid was washed with iPrOH. The crude material contained in the combined filtrate and washings was adsorbed onto Hydromatrix and chromatographed on silica gel [Jones Flashmaster, 20 g/70 mL cartridge, eluting with hexanes: EtOAc 1:1 (1-13)→1:3 (14-38)], yielding the title compound as a yellow foam; 1H NMR (CDCl3, 400 MHz)δ 2.05-2.14 (m, 1H), 2.16-2.28 (m, 1H), 2.50-2.60 (m, 2H), 2.63-2.75 (m, 2H), 3.89 (quint, J=8.4 Hz, 1H), 7.35 (d, J=4.4 Hz, 1H), 7.44 (dd, J=4.2, 8.2 Hz, 1H), 7.55 (d, J=5.2 Hz, 1H), 7.90 (d, J=8.4 Hz, 1H), 8.13 (dd, J=1.6, 8.4 Hz, 1H), 8.22 (d, J=8.2 Hz, 1H), 8.46 (s, 1H), 8.98 (dd, J=1.6, 4.2 Hz, 1H); MS (ES+): m/z 335.1/337.1 (100/44) [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534797B2
Source datasetuspto-grants-2009_05
ORD IDord-73a2b126606b46cb9390502ec8e2d09c
Source noteuspto-grants-2009_05