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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193522Generated: October 31, 2026

4,6-Dichloro-5-methoxypyrimidine → HCID 25070327, compound

https://huagongshe.com/reaction/2193522

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,6-Dichloro-5-methoxypyrimidineHCID 78720—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 59264636HCID 59264636—
Solvent1-ButanolHCID 263—
ProductHCID 25070327HCID 25070327—

Reaction Steps

A mixture of (8-chloro-2-phenylquinolin-3-yl)methanamine (0.035 g, 0.13 mmol) in n-butanol (3 mL) was treated with DIEA (0.046 mL, 0.26 mmol, 2.0 eq) followed with 4,6-dichloro-5-methoxypyrimidine (0.025 g, 0.14 mmol, 1 eq) at 100° C. for 8 h. The reaction mixture was concentrated and purified by column chromatography on a Redi-Sep™ column using 0 to 100% gradient of CH2Cl2:MeOH:NH4OH (89:9:1) in CH2Cl2 as eluent to provide 6-chloro-N-((8-chloro-2-phenylquinolin-3-yl)methyl)-5-methoxypyrimidin-4-amine as a white solid. 1H-NMR (DMSO-d6) δ ppm 8.33 (s, 1H), 8.20 (t, 1H), 8.02-8.04 (m, 1H), 7.99 (s, 1H), 7.93-7.95 (m, 1H), 7.70 (d, J=6.60, 1H), 7.46-7.61 (m, 1H), 4.73 (d, J=5.71, 2H), 2.51 (s, 3H), Mass Spectrum (ESI) m/e=412 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329910B2
Source datasetuspto-grants-2012_12
ORD IDord-18ddc1aeafcd4e438c5679694b166113
Source noteuspto-grants-2012_12