HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 59164499, compound → HCID 59164410, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 59164499 | HCID 59164499 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 59164410 | HCID 59164410 | 8% |
Reaction Steps
A solution of N-[3-(acetyl-methanesulfonyl-amino)-2,4-dioxo-7-trifluoromethyl-1,2,3,4-tetrahydro-quinazolin-6-ylmethyl]-acetamide (305 mg, 0.70 mmol) in 2M aq HCl (5 mL) was stirred at 80° C. for 1 d. Subsequently, the solvent was evaporated and the crude product was purified by preparative thin-layer chromatography (DCM/MeOH 8/2) to yield N-(3-methanesulfonylamino-2,4-dioxo-7-trifluoromethyl-1,2,3,4-tetrahydro-quinazolin-6-ylmethyl)-acetamide (22 mg, 0.056 mmol, 8%) as a light beige solid. 1H-NMR (DMSO-d6, 400 MHz) 3.13 ppm (s, 3H, SO2—CH3); LC-MS rt=2.35 min; MS: m/z 394.9 [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-12d4cd4888ec45439756a4bdd8e2d10c |
| Source note | uspto-grants-2013_08 |