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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894047Generated: October 31, 2026

Diisopropylethylamine → HCID 11965536, compound

https://huagongshe.com/reaction/1894047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanesulfonohydrazideHCID 269268—
ReactantHCID 11965537HCID 11965537—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 11965536HCID 1196553678.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-(4-Chloro-phenoxycarbonylamino)-5-(1-methyl-1H-[1,2,3]triazol-4-yl)-4-trifluoromethyl-benzoic acid methyl ester (260 mg, 0.57 mmol) was dissolved in dioxane (15 mL). After addition of i-Pr2NEt (294 μL, 3 equiv) and CH3SO2NHNH2 (126 mg, 2 equiv), the solution was stirred for 2 h at 100° C. The solvent was removed in vacuo and the crude product was dried in vacuo for 2 h. DCM (5 mL) was then added and, after sonication, the solution was put in the freezer for 16 h. The resulting solid was filtered off, washed with DCM and dried to afford N-[6-(1-methyl-1H-[1,2,3]triazol-4-yl)-2,4-dioxo-7-trifluoromethyl-1,4-dihydro-2H-quinazolin-3-yl]-methanesulfonamide (180 mg, 78%) as an off-white solid. (ESI-MS: m/z 446.5 [M+CH3CN+H]+, rt 3.71 min) 1H-NMR (DMSO-d6, 400 MHz) 8.33 (s, 1H), 8.28 (s, 1H), 7.64 (s, 1H), 4.13 (s, 3H), 3.16 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513268B2
Source datasetuspto-grants-2013_08
ORD IDord-aadf9fc10c0241da9e1422e908dc90c9
Source noteuspto-grants-2013_08