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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441594Generated: November 2, 2026

2,5-Dimethoxytetrahydrofuran → HCID 59164414, compound

https://huagongshe.com/reaction/1441594

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 mn; MS: m/z 402.9 [M+H]+ Column: SunFireC18, 4.6*50 mn, 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 numberUS07655666B2
Source datasetuspto-grants-2010_02
ORD IDord-ba1ef73f87394ebc86f6c06d2ea94937
Source noteuspto-grants-2010_02