Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40693Generated: October 27, 2026

Cesium carbonate → 5-(1H-pyrrolo[2,3-c]pyridin-5-ylamino)pyrazine-2-carbonitrile

https://huagongshe.com/reaction/40693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant5-Aminopyrazine-2-carbonitrileHCID 13925294—
Reactanttert-butyl 5-chloro-1H-pyrrolo[2,3-c]pyridine-1-carboxylateHCID 59636374—
Solvent1,4-DioxaneHCID 31275—
Product5-(1H-pyrrolo[2,3-c]pyridin-5-ylamino)pyrazine-2-carbonitrileHCID 4420464945.4%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of tert-butyl 5-chloro-1H-pyrrolo[2,3-c]pyridine-1-carboxylate (0.030 g, 0.119 mmol), 5-aminopyrazine-2-carbonitrile (0.017 g, 0.142 mmol), cesium carbonate (0.077 g, 0.237 mmol), Xantphos (0.011 g, 0.019 mmol) and tris(benzylideneacetone)dipalladium (0) (0.009 g, 0.010 mmol) in dioxane (0.8 mL) was degassed by bubbling argon through the mixture for 10 minutes. The sealed reaction vessel was heated to 150° C. for 1 hour in a microwave reactor. The crude mixture was filtered through an SCX-2 acidic resin cartridge, eluting with 2 M ammonia in methanol. The basic filtrate was concentrated and purified by column chromatography to give the title compound (0.018 g, 0.054 mmol, 45%). LC-MS (3) Rt=1.30 min; m/z (ESI+) 237 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530468B2
Source datasetuspto-grants-2013_09
ORD IDord-58171aae7fd94b37a68ecf7ba112ffeb
Source noteuspto-grants-2013_09