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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894075Generated: October 30, 2026

2-methyl-2,5-dimethoxytetrahydrofurane → HCID 11965698, compound

https://huagongshe.com/reaction/1894075

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-methyl-2,5-dimethoxytetrahydrofuraneHCID 10920649—
ReactantHCID 59164454HCID 59164454—
SolventAcetic AcidHCID 176—
ProductHCID 11965698HCID 1196569873%

Reaction Steps

To a solution of N-(6-aminomethyl-2,4-dioxo-7-trifluoromethyl-1,4-dihydro-2H-quinazolin-3-yl)-methanesulfonamide (150 mg, 0.43 mmol) in conc. CH3CO2H (10 mL) was added 2-methyl-2,5-dimethoxytetrahydrofurane (62.2 mg, 0.43 mmol) and the reaction mixture was stirred for 2 h at reflux temperature. Subsequently, the solvent was evaporated and the crude light-yellow residue was recrystallized from EtOAc/cyclohexane to yield N-[6-(2-methyl-pyrrol-1-ylmethyl)-2,4-dioxo-7-trifluoromethyl-1,4-dihydro-2H-quinazolin-3-yl]-methanesulfonamide (130 mg, 0.312 mmol, 73%) as a light-orange solid. 1H-NMR (DMSO-d6, 400 MHz) 3.11 ppm (s, 3H, SO2—CH3); LC-MS rt=3.994 nm; MS: m/z 416.9 [M+H]+ Column: SunFireC18, 4.6*50 nm, 3.5 um; Positive MS Water/Acetonitrile 95:5 to 5:95 in 5 min, Flow: 1.5 mL/min

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513268B2
Source datasetuspto-grants-2013_08
ORD IDord-3386292a581d4476be8d1e7236f3ab41
Source noteuspto-grants-2013_08