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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381012Generated: November 2, 2026

Methyl iodide → (4-Methylthio-phenyl)-(2-methyl-quinazolin-4-yl)-methylamine

https://huagongshe.com/reaction/2381012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant(4-Methylthio-phenyl)-(2-methyl-quinazolin-4-yl)-amineHCID 42625835—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(4-Methylthio-phenyl)-(2-methyl-quinazolin-4-yl)-methylamineHCID 1158021743.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (4-methylthio-phenyl)-(2-methyl-quinazolin-4-yl)-amine (263 mg, 0.94 mmol) in DMF (4 ml) at 0° C. was added sodium hydride (56.4 mg, 1.40 mmol, 60% oil dispersion) and followed by methyl iodide (0.09 ml, 1.40 mmol). The mixture was stirred at 0° C. for 1 h, then allowed to warm to room temperature and stirred for another 2 h. The reaction mixture was diluted with EtOAc (15 ml), washed with saturated NaHCO3 aq., brine, dried over Na2SO4, filtered and concentrated by vacuum. The residue was purified by chromatography on silica gel with acetate and hexane (1:2 to 1:1) as eluent, yielding 120 mg of title compound (40.7%). 1H NMR (CDCl3): 7.76 (d, J=9.0 Hz, 1H), 7.54 (t, J=7.5 Hz, 1H), 7.24-7.19 (m, 2H), 7.10-6.97 (m, 4H), 3.59 (s, 3H), 2.74 (s, 3H), 2.48 (s, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258145B2
Source datasetuspto-grants-2012_09
ORD IDord-680a45d5366946a1b0cd9185001409e5
Source noteuspto-grants-2012_09