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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716042Generated: October 26, 2026

Cesium carbonate → HCID 71015501, compound

https://huagongshe.com/reaction/716042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant(6-Aminopyridin-3-yl)methanolHCID 2794829—
Reactant1-(2-bromo-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-yl)-2,2-dimethylpropane-1-oneHCID 57829221—
Catalystpalladium(II) acetateHCID 167845—
CatalystBinap, (A+-)-HCID 634876—
SolventTolueneHCID 1140—
ProductHCID 71015501HCID 7101550145.3%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a 35 ml seal tube, 1-(2-bromo-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-yl)-2,2-dimethylpropane-1-one (1.0 g, 0.00242 mole) and (6-aminopyridin-3-yl)methanol (0.36 g, 0.00291 mole) was taken in toluene (10.0 ml). The reaction mixture was purged with argon for 15 min at RT followed by Cs2CO3 (3.1 g, 0.0097 mole) was added and further purged for 30 min with argon. BINAP (0.03 g, 0.000048 mole) and Pd(OAc)2 (0.01 g, 0.000048 mole) were added and the reaction mixture was heated to 110° C. for 16 hrs. After completion of the reaction, the reaction mixture was filtered through celite bed and washed with ethyl acetate. Filtrate was collected and concentrated to afford crude product which was purified using column purification by eluting the compound with 20-25% ethyl acetate in hexanes to yield 0.5 g of 1-(2-(5-(hydroxymethyl)pyridin-2-ylamino)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazin-7-yl)-2,2-dimethylpropan-1-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187487B2
Source datasetuspto-grants-2015_11
ORD IDord-f27ab9846c1a426e98a233075ab22e35
Source noteuspto-grants-2015_11