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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627685Generated: October 29, 2026

Nitrogen → 2-Pyridinecarboxylic acid, 3-chloro-5-cyano-, 1,1-dimethylethyl ester

https://huagongshe.com/reaction/627685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
Reactanttert-Butyl 5-bromo-3-chloropyridine-2-carboxylateHCID 68109709—
ReactantHCID 178514179HCID 178514179—
CatalystZincHCID 23994—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDimethylformamideHCID 6228—
Product2-Pyridinecarboxylic acid, 3-chloro-5-cyano-, 1,1-dimethylethyl esterHCID 86728141—

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of tert-butyl 5-bromo-3-chloropicolinate (12 g, 41.0 mmol), dicyanozinc (3.37 g, 28.7 mmol), and zinc (0.375 g, 5.74 mmol) were suspended in DMF (82 ml) in round bottom flak. The suspension was purged with N2 and finally Pd2(dba)3 (1.878 g, 2.051 mmol), tri-tert-butylphosphine (6.2 ml, 6.15 mmol) and neat tri-tert-butylphosphine (300 mg), was added under the Ar. The r×n mixture was heated to 95° C. for 3 h. Then another 2.8 g of Pd2(dba)3 and 1.2 g of neat P ligand were added. 3.5 h later, it was cooled to RT and black precipitate was filtered out by filtration. The filtrate was diluted with 150 ml of MTBE. The organic layer was washed with 100 ml of water and brine. It was dried on MgSO4 and concentrated which was carried over to next step directly. MS m/z=261.0/263.0 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309263B2
Source datasetuspto-grants-2016_04
ORD IDord-284939929b5746f68d90bb24f8fc1ce9
Source noteuspto-grants-2016_04