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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906569Generated: October 30, 2026

2,5-Dimethoxytetrahydrofuran → HCID 59164414, compound

https://huagongshe.com/reaction/906569

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 numberUS08012988B2
Source datasetuspto-grants-2011_09
ORD IDord-0b871249b5e14b77881607cf82fc1f4e
Source noteuspto-grants-2011_09