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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092541Generated: October 25, 2026

Dimethylformamide → 5-[7-(3-Methanesulfonyl-phenyl)-4-morpholin-4-yl-quinazolin-2-yl]-pyridin-2-ylamine

https://huagongshe.com/reaction/2092541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCesium carbonateHCID 10796—
Reactant5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amineHCID 2756555—
Reactant4-(2-Chloro-7-(3-(methylsulfonyl)phenyl)quinazolin-4-yl)morpholineHCID 86665760—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
Product5-[7-(3-Methanesulfonyl-phenyl)-4-morpholin-4-yl-quinazolin-2-yl]-pyridin-2-ylamineHCID 6751442874%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a 50 mL round bottom flask, 2-chloro-7-(3-methanesulfonyl-phenyl)-4-morpholin-4-yl-quinazoline (0.15 g, 0.00037 mol), 2-aminopyridine-5-boronic acid pinacol ester (0.122 g, 0.0005568 mol), cesium carbonate (0.243 g, 0.00074 mol), DMF (4 mL) and water (2 mL) were added. The reaction mixture was degassed with nitrogen for 5-10 min. To the same reaction flask, Pd(PPh3)2Cl2 (0.013 g, 0.000018 mol) was added and again degassed with nitrogen for 5-10 min. The reaction mixture was stirred at 95° C. for 2 h. The reaction mixture was cooled and diluted with ethyl acetate. The organic layer was washed with water, brine and dried over sodium sulfate. The solvent was removed under reduced pressure to afford the crude product. The crude product was purified using column chromatography (60-120 silica gel, 5% MeOH in chloroform) to yield the title compound (125 mg, 74%). LC-MS (ESI): Calculated mass: 461.2; Observed mass: 462.1 [M+H]+ (RT: 0.17 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440662B2
Source datasetuspto-grants-2013_05
ORD IDord-d1be9849c5e84fdf8b2b739665d8df77
Source noteuspto-grants-2013_05