HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894074Generated: October 30, 2026
2,5-Dimethoxytetrahydrofuran → HCID 59164414, compound
https://huagongshe.com/reaction/1894074
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,5-Dimethoxytetrahydrofuran | HCID 79098 | — |
| Reactant | HCID 59164454 | HCID 59164454 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 59164414 | HCID 59164414 | 96.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08513268B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-e53992bd8cd64517a0846d96325f8e88 |
|---|
| Source note | uspto-grants-2013_08 |
|---|