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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869116Generated: October 31, 2026

2-(Dimethylamino)ethanol → Allyl 2-amino-5-(2-(dimethylamino)ethoxy)pyrazolo[1,5-a]pyrimidine-3-carboxylate

https://huagongshe.com/reaction/869116

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dimethylamino)ethanolHCID 7902—
ReactantCesium carbonateHCID 10796—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantBenzotriazol-1-yl-oxytripyrrolidinophosphoniumHCID 2724700—
Reactantallyl 2-amino-5-oxo-4H-pyrazolo[1,5-a]pyrimidine-3-carboxylateHCID 136629519—
SolventAcetonitrileHCID 6342—
ProductAllyl 2-amino-5-(2-(dimethylamino)ethoxy)pyrazolo[1,5-a]pyrimidine-3-carboxylateHCID 9041200735%

Reaction Steps

To a mixture of allyl 2-amino-5-oxo-4H-pyrazolo[1,5-a]pyrimidine-3-carboxylate (1 g, 4.270 mmol) in MeCN (15 mL) was added 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine (975.1 mg, 957.9 μL, 6.405 mmol) and benzotriazol-1-yloxy(tripyrrolidin-1-yl)phosphonium (Phosphorus Hexafluoride Ion) (2.666 g, 5.124 mmol). After 5 minutes, 2-dimethylaminoethanol (3.806 g, 4.291 mL, 42.70 mmol) and cesium carbonate (5 g) were added and the mixture was stirred at room temperature for 30 minutes, followed by heating to 50° C. for 30 minutes. After cooling to room temperature the mixture was filtered and the solid washed with acetonitrile. The combined filtrate was concentrated in vacuo to an orange oil and purified by column chromatography using 4% MeOH/DCM as eluent to provide 4b (yield 35%) LC-MS (M+H)+=306.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969360B2
Source datasetuspto-grants-2015_03
ORD IDord-a77d5a4da886420bafe34033ce007b6b
Source noteuspto-grants-2015_03