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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390866Generated: October 25, 2026

Lithium Chloride → 6-{(E)-2-[3-tert-butyl-5-(5-fluoro-2-methoxy-pyridin-3-yl)-2-methoxy-phenyl]-vinyl}-pyridin-3-ylamine

https://huagongshe.com/reaction/2390866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium ChlorideHCID 433294—
ReactantTris(furan-2-yl)phosphaneHCID 521585—
Reactant6-Iodopyridin-3-amineHCID 2320576—
Reactant3-[3-tert-Butyl-4-methoxy-5-((E)-2-tributylstannanyl-vinyl)-phenyl]-5-fluoro-2-methoxy-pyridineHCID 59156634—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product6-{(E)-2-[3-tert-butyl-5-(5-fluoro-2-methoxy-pyridin-3-yl)-2-methoxy-phenyl]-vinyl}-pyridin-3-ylamineHCID 6728655487.1%

Reaction Conditions

Temperature110 °C

Reaction Steps

step 1—A solution of Pd2(dba)3 (27.8 mg, 0.030 mmol) and tris-(2-furyl)phosphine (28.0 mg, 0.121 mmol) in anhydrous DMF (3 mL) was stirred at RT for 15 min under argon. To the resulting solution was added via cannula a solution of 364 (672 mg, 1.11 mmol) and 2-iodo-5-aminopyridine (294 mg, 1.33 mmol) in anhydrous DMF (6 mL) at RT. Lithium chloride (97.1 mg, 2.23 mmol) was then added under argon. The reaction mixture was heated at 110° C. for 18 h. After cooling to RT, the reaction mixture was poured into H2O (90 mL) and thrice extracted with EtOAc (60 mL). The combined extracts were washed with H2O (130 mL) and brine (130 mL), dried (Na2SO4), filtered and concentrated. The crude product was purified by SiO2 chromatography eluting with an EtOAc/hexane gradient (37 to 100% EtOAc) to afford 0.394 g (85%) of 6-{(E)-2-[3-tert-butyl-5-(5-fluoro-2-methoxy-pyridin-3-yl)-2-methoxy-phenyl]-vinyl}-pyridin-3-ylamine (370).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273773B2
Source datasetuspto-grants-2012_09
ORD IDord-42ea3b71795c45409c2aecd0923e8963
Source noteuspto-grants-2012_09