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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385038Generated: November 1, 2026

Ammonia → 8-Bromoquinoline-5-carbonitrile

https://huagongshe.com/reaction/1385038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantUreaHCID 1176—
ReactantSodium CyanideHCID 8929—
Reactant8-Bromoquinolin-5-amineHCID 12950054—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 178424363HCID 178424363—
CatalystCopper SulfateHCID 24462—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product8-Bromoquinoline-5-carbonitrileHCID 18403026—

Reaction Steps

0.60 g of concentrated hydrochloric acid was added dropwise to a mixture of 0.70 g of 5-amino-8-bromoquinoline and 3.15 ml of acetic acid, and the mixture was stirred for 1 hour at room temperature. At 0-50° C., 0.22 g of sodium nitrite in 0.45 ml of water were then added, and the mixture was stirred for 1 hour. After the addition of 20 mg of urea in 0.16 ml of water, stirring was continued at 0-50° C. for a further hour. This solution is added to a two-phase system of toluene/copper(I) cyanide solution which was prepared as follows: a solution of 0.79 g of copper(II) sulfate in 2.2 ml of water was added dropwise to a solution of 1.06 g of 10% strength ammonia solution and 0.77 g of sodium cyanide, and 6 ml of toluene were added to this mixture to form a lower layer. After stirring for 1 hour at room temperature, insoluble particles were filtered off and the solution was extracted with ethyl acetate. The organic phase was dried and the solvent was removed under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262074B1
Source datasetuspto-grants-2001_07
ORD IDord-3db926f72e2f4320ac2c9690aeba2310
Source noteuspto-grants-2001_07