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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064313Generated: October 30, 2026

3-Methoxypropylamine → 1,2-Dimethylimidazol-5-yl-2-{4-[N-(2-mesylethyl)sulphamoyl]anilino}pyrimidine

https://huagongshe.com/reaction/1064313

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxypropylamineHCID 1672—
Reactant4-(1,2-Dimethylimidazol-5-yl)-2-(4-(fluorosulphonyl)anilino)pyrimidineHCID 22273505—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1,2-Dimethylimidazol-5-yl-2-{4-[N-(2-mesylethyl)sulphamoyl]anilino}pyrimidineHCID 69665794161.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-Dimethylaminopyridine (3 mg, 0.025 mmol) and 3-methyoxypropylamine (200 μl, 2 mmol) were added to a solution of 4-(1,2-dimethylimidazol-5-yl)-2-(4-(fluorosulphonyl)anilino)pyrimidine (Method 59; 87 mg, 0.25 mmol) in NMP (1 mL) and the mixture heated at 100° C. for 18 hours. The mixture was allowed to cool to ambient temperature and the solvent removed by evaporation. The residue was purified by preparative LCMS (constant flow of 5% v/v (35% NH3 in MeOH) with a gradient of H2O:CH3CN (5:95 increasing in polarity to 95:5) over 7.5 min) to give the title compound (91 mg, 81%) as a solid. NMR 2.38 (s, 3H), 2.97 (s, 3H), 3.11 (m, 2H), 3.21 (m, 2H), 3.95 (s, 3H), 7.20 (d, 1H), 7.61 (s, 1H), 7.75 (m, 3H), 7.95 (d, 2H), 8.43 (d, 1H), 9.95 (s, 1H); m/z 451.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969714B2
Source datasetuspto-grants-2005_11
ORD IDord-5ba85213a1304ef79839f1ab60ac58a3
Source noteuspto-grants-2005_11