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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377842Generated: November 1, 2026

2-Aminobenzonitrile → HCID 178482916, compound

https://huagongshe.com/reaction/2377842

Reaction equation

Participants

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

Reaction Steps

LiHMDS (3.5 equivalents) was added to ethyl {5-[3-(dimethylamino)pyrrolidin-1-yl]-3H-imidazo[4,5-b]pyridin-2-yl}acetate (1.0 equivalent) in THF at −40° C. After 10 minutes, a solution of 2-aminobenzenecarbonitrile (1.1 equivalents) in THF was added. The resulting mixture was allowed to warm to room temperature, stirred for 1 hour, and then heated to 60° C. overnight. The mixture was cooled to room temperature and quenched with NH4Cl (aqueous saturated). The aqueous phase was extracted with CH2Cl2 (5 times). The product crashed 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+), Rt 1.48 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470709B2
Source datasetuspto-grants-2008_12
ORD IDord-cf7ffb07a90b4ed7840d4bad222f89ae
Source noteuspto-grants-2008_12