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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894074Generated: October 30, 2026

2,5-Dimethoxytetrahydrofuran → HCID 59164414, compound

https://huagongshe.com/reaction/1894074

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DimethoxytetrahydrofuranHCID 79098—
ReactantHCID 59164454HCID 59164454—
SolventAcetic AcidHCID 176—
ProductHCID 59164414HCID 5916441496.4%

Reaction Steps

To a solution of N-(6-aminomethyl-2,4-dioxo-7-trifluoromethyl-1,4-dihydro-2H-quinazolin-3-yl)-methanesulfonamide (100 mg, 0.28 mmol) in conc. CH3CO2H (8 mL) was added 2,5-dimethoxytetrahydrofurane (41.3 μL, 0.31 mmol) and the reaction mixture was stirred for 20 min at reflux temperature. Subsequently, the solvent was evaporated and the crude brown residue was recrystallized from EtOAc/cyclohexane to yield N-(2,4-dioxo-6-pyrrol-1-ylmethyl-7-trifluoromethyl-1,4-dihydro-2H-quinazolin-3-yl)-methanesulfonamide (108 mg, 0.27 mmol, 95%) as a light-brown solid. 1H-NMR (DMSO-d6, 400 MHz) 3.12 ppm (s, 3H, SO2—CH3); LC-MS rt=3.757 nm; MS: m/z 402.9 [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-e53992bd8cd64517a0846d96325f8e88
Source noteuspto-grants-2013_08