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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098011Generated: October 27, 2026

methyl 2-(7-bromo-2-oxoquinolin-1(2H)-yl)acetate → methyl 2-(7-cyano-2-oxoquinolin-1(2H)-yl)acetate

https://huagongshe.com/reaction/2098011

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 2-(7-bromo-2-oxoquinolin-1(2H)-yl)acetateHCID 68784498—
ReactantHCID 178418546HCID 178418546—
CatalystHCID 178418397HCID 178418397—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Productmethyl 2-(7-cyano-2-oxoquinolin-1(2H)-yl)acetateHCID 6878545171.4%

Reaction Steps

CuCN (0.211 g, 2.36 mmol) and Pd(PPh3)4 (0.136 g, 0.118 mmol) were added to a solution of methyl 2-(7-bromo-2-oxoquinolin-1(2H)-yl)acetate (0.35 g, 1.18 mmol) in DMF (1 mL) in a screw cap vial. The vial was sealed and placed into a oil bath at 120° C. and the reaction mixture was stirred for 18 h. The resulting mixture was diluted with Et2O and washed with brine. The organic phase was separated, dried (Na2SO4), filtered, concentrated under vacuum and the residue was purified on a silica gel column to give methyl 2-(7-cyano-2-oxoquinolin-1(2H)-yl)acetate (0.204 g, 71%). Retention time (min)=1.464, method [1], MS (ESI) 243.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450363B2
Source datasetuspto-grants-2013_05
ORD IDord-e7dbe15ad3dd49bca7d36fe9e3782576
Source noteuspto-grants-2013_05