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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923695Generated: November 2, 2026

Sodium Chloride → methyl 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1H-indol-6-yl)pyridine-2-carboxylate

https://huagongshe.com/reaction/923695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantCesium fluorideHCID 25953—
ReactantMethyl 4-amino-3,6-dichloro-5-fluoropicolinateHCID 22677265—
Reactant7-Fluoro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(triisopropylsilyl)-1H-indoleHCID 90418659—
CatalystHCID 178418476HCID 178418476—
SolventEthyl AcetateHCID 8857—
SolventAcetonitrile--water (1/1)HCID 18373917—
Productmethyl 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1H-indol-6-yl)pyridine-2-carboxylateHCID 7831909154.3%

Reaction Conditions

Temperature115 °C

Reaction Steps

7-fluoro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(triisopropylsilyl)-1H-indole (500 mg, 1.2 mmol), methyl 4-amino-3,6-dichloro-5-fluoropicolinate (290 mg, 1.2 mmol), cesium fluoride (360 mg, 2.4 mmol) and bis(triphenylphosphine)palladium(II) chloride (84 mg, 0.12 mmol) were combined in 4 mL of a 1:1 v/v acetonitrile-water and heated at 115° C. for 25 min in a Biotage Initiator microwave reactor. The mixture was partitoned between ethyl acetate and sat. NaCl and the organic phase was dried and evaporated. Purification by flash chromatography (SiO2; eluting with 0-20% ethyl acetate in dichloromethane) provided impure product. The material was purified by flash chromatography again (SiO2; eluting with 0-30% ethyl acetate in hexanes) to provide the title compound as a white solid (220 mg, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278985B2
Source datasetuspto-grants-2016_03
ORD IDord-08eba69f9cac4baaa134835ba417ef85
Source noteuspto-grants-2016_03