HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906570Generated: October 30, 2026
2-methyl-2,5-dimethoxytetrahydrofurane → HCID 11965698, compound
https://huagongshe.com/reaction/906570
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-methyl-2,5-dimethoxytetrahydrofurane | HCID 10920649 | — |
| Reactant | HCID 59164454 | HCID 59164454 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 11965698 | HCID 11965698 | 73% |
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 mn; MS: m/z 416.9 [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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012988B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-3c61fd1c41e449a18145107de291791a |
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| Source note | uspto-grants-2011_09 |
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