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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850667Generated: October 30, 2026

Water → Allyl 2-amino-6-fluoro-pyrazolo[1,5-a]pyrimidine-3-carboxylate

https://huagongshe.com/reaction/1850667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-(Diisopropylamino)-2-fluoro-prop-2-enalHCID 72741393—
ReactantAllyl 3,5-diamino-1H-pyrazole-4-carboxylateHCID 73554792—
SolventDimethyl SulfoxideHCID 679—
ProductAllyl 2-amino-6-fluoro-pyrazolo[1,5-a]pyrimidine-3-carboxylateHCID 86720887—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspension of allyl 3,5-diamino-1H-pyrazole-4-carboxylate 3 (42.72 g, 234.5 mmol) in DMSO (270.8 mL)/Water (270.8 mL), was added p-TsOH hydrate (46.72 g, 245.6 mmol) and 3-(diisopropylamino)-2-fluoro-prop-2-enal (described in Tetrahedron Letters, 33(3), 357-60; 1992) (38.69 g, 223.3 mmol). The reaction mixture was heated to 100° C. for 3 h during which time a solid slowly precipitated out of solution. The orange suspension was allowed to cool down to RT overnight. The solid was filtered, washed with water and dried under vacuum to give allyl 2-amino-6-fluoro-pyrazolo[1,5-a]pyrimidine-3-carboxylate 4a as a sand solid (45.05 g, 85% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957078B2
Source datasetuspto-grants-2015_02
ORD IDord-d20a804d6b3f4546ba023b12f3525b54
Source noteuspto-grants-2015_02