Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930503Generated: October 28, 2026

P-Anisidine → US9296747, Example 5

https://huagongshe.com/reaction/930503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantEthyl AcetateHCID 8857—
Reactant(2-Chloro-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)(pyridin-3-yl)methanoneHCID 118970896—
SolventIsopropanolHCID 3776—
ProductUS9296747, Example 5HCID 11897090924.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of (2-chloro-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)(pyridin-3-yl)methanone, Intermediate 5 (0.025 g, 0.091 mmol) in isopropanol (0.1 mL) was treated with 4-methoxyaniline (0.018 g, 0.100 mmol). The resulting mixture was heated to 60° C. and allowed to stir overnight. After being allowed to cool to room temperature EtOAc (10 mL) was added to the reaction mixture, and the resulting solution was then washed twice with brine (10 mL). The combined aqueous layers were washed once with EtOAc (10 mL). The organic layers were combined, then dried over anhydrous Na2SO4(s), filtered and concentrated in vacuo. The resulting crude residue was then purified over silica using a MeOH/CHCl3 gradient. The desired product was obtained in 24.3% yield (0.008 g, 0.024 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296747B1
Source datasetuspto-grants-2016_03
ORD IDord-74894cb051154347b24e8898a8619561
Source noteuspto-grants-2016_03