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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71330Generated: October 26, 2026

2,4-Dichloro-5-fluoropyrimidine → HCID 178505996, compound

https://huagongshe.com/reaction/71330

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-5-fluoropyrimidineHCID 250705—
ReactantHCID 178507542HCID 178507542—
SolventMethanol--water (1/1)HCID 22242641—
ProductHCID 178505996HCID 178505996—

Reaction Steps

A reaction mixture containing 2,4-dichloro-5-fluoro-pyrimindine (1.2 equivalents) and 3-(tetrazol-5-yl)aniline (1 equivalents) in methanol:water (1:1; v/v) was heated at 60° C. for 24 h. Upon dilution with water and acidification, the solid formed was filtered, washed with water, dried and analyzed to give 2-chloro-5-fluoro-N4-[3-(1H-tetrazol-5-yl)phenyl]-4-pyrimidineamine (R926853). Alternatively this reaction can be achieved by treating 2,4-dichloro-5-fluoropyrimidine (1 equivalent) with 3-(tetrazol-5-yl)aniline (3 equivalents) in methanol:water (1:1; v/v) at 60° C. for 2-3 hours or at room temperature for 24 h to give 2-chloro-5-fluoro-N4-[3-(1H-tetrazol-5-yl)phenyl]-4-pyrimidineamine. 1H NMR (DMSO-d6): δ 10.25 (s, 1H), 8.43 (s, 1H), 8.37 (d, 1H, J=3.6 Hz), 7.90 (dd, 1H, J=0.9 and 9 Hz), 7.75 (d, 1H, J=7.5 Hz), 7.61 (t, 1H, J=7.8 Hz); LCMS: purity: 90%; MS (m/e): 292 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822685B2
Source datasetuspto-grants-2014_09
ORD IDord-d7937c8d8a9e4f72806f0d92b9ece95e
Source noteuspto-grants-2014_09