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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271218Generated: October 26, 2026

Cesium carbonate → 2-Furancarboxamide, N-[2-methyl-4-(1-pyrrolidinyl)-7-quinazolinyl]-

https://huagongshe.com/reaction/1271218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1,2-Diaminocyclohexane, trans-HCID 43806—
ReactantFuramideHCID 69108—
Reactant7-Bromo-2-methyl-4-pyrrolidin-1-yl-quinazolineHCID 22474939—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
Product2-Furancarboxamide, N-[2-methyl-4-(1-pyrrolidinyl)-7-quinazolinyl]-HCID 997341922%

Reaction Steps

A suspension of 0.12 g (0.41 mmol) of 7-bromo-2-methyl-4-pyrrolidin-1-yl-quinazoline, 3.9 mg (0.021 mmol) of copper (I) iodide and 0.267 g (0.82 mmol) of caesium carbonate in dioxane (5 ml) was treated at RT under argon with 4.7 mg (0.041 mmol) of trans-1,2-diaminocyclohexane and 0.18 g (1.6 mmol) of 2-furamide and then heated at reflux under argon for 20 h. The reaction mixture was partitioned between EtOAc and water, the layers were separated, the organic layer washed twice with water dried over sodium sulphate and concentrated in vacuo. The residue was applied to silica gel column with CH2Cl2/MeOH/NH4OH (9:1:0.5) as eluent. Combination of the purified fractions and concentration in vacuo gave 29 mg (22%) of the furan-2-carboxylic acid (2-methyl-4-pyrrolidin-1-yl-quinazolin-7-yl)-amide as an off white solid. ISP mass spectrum, m/e: 323.4 (M+1 calculated for C18H18N4O2: 323).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205309B2
Source datasetuspto-grants-2007_04
ORD IDord-daf25bfb61484ba7bd434f4615e8a6ba
Source noteuspto-grants-2007_04