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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395352Generated: November 3, 2026

2-Aminobenzonitrile → HCID 178482916, compound

https://huagongshe.com/reaction/395352

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobenzonitrileHCID 72913—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 178470770HCID 178470770—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178482916HCID 178482916—

Reaction Steps

LiHMDS (3.5 eq) was added to ethyl {5-[3-(dimethylamino)pyrrolidin-1-yl]-3H-imidazo[4,5-b]pyridin-2-yl}acetate (1.0 eq) in THF at −40° C. After 10 minutes, a solution of 2-aminobenzenecarbonitrile (1.1 eq) in THF was added. The resulting mixture was allowed to warm to room temperature, stirred for 1 h and then heated to 60° C. overnight. The mixture was cooled to room temperature and quenched with NH4Cl (aq, saturated). The aqueous phase was extracted with CH2Cl2 (5 times). The product crashes out of the organic solution during the extractions. Evaporation of the solvent under reduced pressure afforded a brown solid that was triturated repeatedly with MeOH and acetone to obtain a yellow greenish powder. LC/MS m/z 390.2 (MH+), Rf 1.48 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605617B2
Source datasetuspto-grants-2003_08
ORD IDord-6ce4b96b2bfc44c89ddeed4005f992bb
Source noteuspto-grants-2003_08