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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876132Generated: November 2, 2026

Sodium methanethiolate → (2-Methylthio-quinazolin-4-yl)-(4-methoxy-phenyl)-methyl-amine

https://huagongshe.com/reaction/1876132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
Reactant2-chloro-N-(4-methoxyphenyl)-N-methylquinazolin-4-amineHCID 11738112—
SolventEthyl AcetateHCID 8857—
Product(2-Methylthio-quinazolin-4-yl)-(4-methoxy-phenyl)-methyl-amineHCID 117713367.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of (2-chloro-quinazolin-4-yl)-(4-methoxy-phenyl)-methyl-amine (150 mg, 0.5 mmol), sodium methanethiolate (105 mg, 1.5 mmol) in 5 mL of solvent (THF:MeOH:water=3:1:1) was stirred at 70° C. for 4 h. The reaction mixture was diluted with 30 mL of ethyl acetate and it was washed with brine, dried over anhydrous Na2SO4, filtered and concentrated. The crude product was purified by chromatography on silica gel with acetate and hexane (1:5) as eluent, yielding 11 mg of title compound (7%). 1H NMR (CDCl3): 7.65 (d, J=8.4 Hz, 1H), 7.51-7.45 (m, 1H), 7.14-7.10 (m, 2H), 6.93-6.89 (m, 4H), 3.84 (s, 3H), 3.58 (s, 3H), 2.67 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309562B2
Source datasetuspto-grants-2012_11
ORD IDord-bc95609a8dfd45eebccae7e5e1b1bd29
Source noteuspto-grants-2012_11