Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395350Generated: October 29, 2026

2-Aminobenzonitrile → HCID 178507210, compound

https://huagongshe.com/reaction/395350

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobenzonitrileHCID 72913—
ReactantHCID 22664674HCID 22664674—
ProductHCID 178507210HCID 178507210—

Reaction Steps

The title compound was synthesized as described in Example 45, Method E using ethyl 2-(5-morpholin-4-ylimidazolo[5,4-b]pyridin-2-yl)acetate and 2-aminobenzenecarbonitrile, with a modified workup procedure. After quenching with a saturated aqueous ammonium chloride solution, the two phases were separated and the aqueous phase extracted with EtOAc. Upon standing, a solid formed and precipitated out of the organic extracts. The precipitate, a dark brown solid, was filtered off and dried. Purification by reverse phase chromatography afforded the desired product as a reddish solid. LC/MS m/z 363.2 (MH+), Rf 2.20 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605617B2
Source datasetuspto-grants-2003_08
ORD IDord-32060f59face4359aa9f59f3d7fec8d1
Source noteuspto-grants-2003_08