Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924148Generated: October 26, 2026

Potassium Phosphate, Tribasic → (R)-N-(4-(Chlorodifluoromethoxy)phenyl)-5-(2-cyano-5-fluorophenyl)-6-(3-hydroxypyrrolidin-1-yl)nicotinamide

https://huagongshe.com/reaction/924148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrileHCID 22180788—
Reactant(R)-5-Bromo-N-(4-(chlorodifluoromethoxy)phenyl)-6-(3-hydroxypyrrolidin-1-yl)nicotinamideHCID 72545856—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Product(R)-N-(4-(Chlorodifluoromethoxy)phenyl)-5-(2-cyano-5-fluorophenyl)-6-(3-hydroxypyrrolidin-1-yl)nicotinamideHCID 89908257—

Reaction Conditions

Temperature120 °C

Reaction Steps

(R)-5-Bromo-N-(4-(chlorodifluoromethoxy)phenyl)-6-(3-hydroxypyrrolidin-1-yl)nicotinamide (Stage 171.1, 50 mg, 0.108 mmol), 4-fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile (32 mg, 0.130 mmol), PdCl2(dppf) (7.91 mg, 10.81 μmol) and K3PO4 (68.8 mg, 0.324 mmol) were added to a vial and flushed with argon. Dioxane (1 mL) was added and the mixture was stirred at 120° C. for 1.5 h. The solvent was evaporated off under reduced pressure and the crude product was purified by preparative SFC (Column 2-EP, from 17% to 22% in 6 min). The purified product was lyophilized in water/min. vol. MeCN to afford the title product as a slightly yellow powder. UPLC-MS (Condition 3), tR=1.09 min, m/z=503.1/505.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278981B2
Source datasetuspto-grants-2016_03
ORD IDord-44095c70907f4b2dbb10e360f19caaf4
Source noteuspto-grants-2016_03