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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335957Generated: October 30, 2026

Potassium Phosphate, Tribasic → HCID 86658496, compound

https://huagongshe.com/reaction/335957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Fluoropyridine-3-boronic acidHCID 2783270—
ReactantHCID 86658497HCID 86658497—
CatalystBis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)HCID 11714597—
ProductHCID 86658496HCID 8665849683%

Reaction Steps

A vial was charged with tert-butyl 7-bromo-3-chloro-5′H-spiro[chromeno[2,3-c]pyridine-5,4′-thiazole]-2′-ylcarbamate (0.250 g, 0.518 mmol), 2-fluoropyridin-3-ylboronic acid (0.15 g, 1.04 mmol), potassium phosphate (0.33 g, 1.55 mmol) and bis-(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) (0.018 g, 0.026 mmol). The vial was sealed before evacuating and backfilling with nitrogen. The solids were suspended in 1,4-dioxane (2.22 mL) and water (0.37 mL). The vial was placed in a pre-heated 100° C. oil bath. The reaction was stirred for 1 h before cooling to RT. The reaction was diluted with water (30 mL) and extracted with ether (2×50 mL). The combined organic layers were washed sequentially with water and brine before drying over sodium sulfate. The solvent was removed under reduced pressure and the crude material was purified by silica gel chromatography to afford tert-butyl 3-chloro-7-(2-fluoropyridin-3-yl)-5′H-spiro[chromeno[2,3-c]pyridine-5,4′-thiazole]-2′-ylcarbamate (0.21 g, 0.43 mmol, 83% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883782B2
Source datasetuspto-grants-2014_11
ORD IDord-da137530ebbd4970a2a586dbc33fff0d
Source noteuspto-grants-2014_11