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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493791Generated: October 30, 2026

HCID 53629051, compound → HCID 53629050, compound

https://huagongshe.com/reaction/493791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 53629051HCID 53629051—
SolventPhosphorus oxychlorideHCID 24813—
ProductHCID 53629050HCID 53629050—

Reaction Steps

N-[(3-chloropyrazin-2-yl)(3-phenylquinoxalin-6-yl)methyl]-cyclobutanecarboxamide (56 mg, 0.13 mmol) was heated in POCl3 (5 mL) under Ar at 70° C. for 26 h. Later the reaction was cooled to rt, evaporated under reduced pressure and then high vacuum. A solution of NH3 in i-PrOH (2 M, 10 mL was added to the crude material cooled in an ice-H2O bath under Ar. The mixture was stirred, sonicated and filtered. The solids and the reaction flask were washed with i-PrOH multiple times. The filtrate was concentrated under reduced pressure. The light yellow residue was partitioned between DCM (60 mL) and H2O (20 mL). The aq. layer was extracted with DCM (2×). Combined organic phase was washed with brine and dried (Na2SO4) to afford the title compound as a light yellow solid; 1H NMR (400 MHz, CD3CN) δ 9.40 (s, 1H), 8.36 (s, 1H), 8.32-8.25 (m, 2H), 8.13-8.11 (m, 2H), 7.77 (d, J=4.8 Hz, 1H), 7.63-7.51 (m, 3H), 7.32 (d, J=4.8 Hz, 1H), 3.97 (qund, J=1.2 Hz, 8.4 Hz, 1H), 2.60-2.45 (m, 4H), 2.05-1.95 (m, 2H). MS (ES+): m/z 412.0 (40) [MH+]; HPLC: tR=4.10 min (OpenLynx, polar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534797B2
Source datasetuspto-grants-2009_05
ORD IDord-5c439a668ed2491f9b291dab9aa6b6dc
Source noteuspto-grants-2009_05