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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930534Generated: October 26, 2026

Water → tert-butyl 4-((2-hydroxyethyl)(phenyl)amino)-2-(4-(oxazol-5-yl)phenylamino)-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate

https://huagongshe.com/reaction/1930534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-(2-Hydroxyethyl)anilineHCID 31235—
Reactanttert-butyl 2-(4-(oxazol-5-yl)phenylamino)-4-(trifluoromethylsulfonyloxy)-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylateHCID 59333731—
SolventDimethyl SulfoxideHCID 679—
Producttert-butyl 4-((2-hydroxyethyl)(phenyl)amino)-2-(4-(oxazol-5-yl)phenylamino)-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylateHCID 5933371977%

Reaction Conditions

Temperature70 °C

Reaction Steps

2-(Phenylamino)ethanol (0.051 g, 0.37 mmol) was added to tert-butyl 2-(4-(oxazol-5-yl)phenylamino)-4-(trifluoromethylsulfonyloxy)-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate (0.2 g, 0.37 mmol, Example 1b) in DMSO (3 mL). The reaction mixture was heated in a microwave reactor at 70° C. for 3 h. Water (1 mL) was added to the solution and the precipitate was washed with water and filtered to give tert-butyl 4-((2-hydroxyethyl)(phenyl)amino)-2-(4-(oxazol-5-yl)phenylamino)-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate (150 mg, 77%). No further purification. MS (ESI+)/(ESI−) m/z 529/527

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188101B2
Source datasetuspto-grants-2012_05
ORD IDord-970073b353b84590b65f44327164f120
Source noteuspto-grants-2012_05