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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626747Generated: October 31, 2026

Potassium Phosphate, Tribasic → [2-(2,6-dichlorophenyl)-7-fluoro-2H-pyrazolo[4,3-c]pyridin-4-yl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/626747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactanttert-Butyl carbamateHCID 77922—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant4-Bromo-2-(2,6-dichlorophenyl)-7-fluoro-2H-pyrazolo[4,3-c]pyridineHCID 86697056—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product[2-(2,6-dichlorophenyl)-7-fluoro-2H-pyrazolo[4,3-c]pyridin-4-yl]-carbamic acid tert-butyl esterHCID 6967490257%

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspension of 4-bromo-2-(2,6-dichlorophenyl)-7-fluoro-2H-pyrazolo[4,3-c]pyridine (635 mg, 1.75 mmol), tert-butyl carbamate (614 mg, 5.25 mmol), Pd2(dba)3 (40 mg, 0.044 mmol), Xantphos (101 mg, 0.175 mmol) and potassium phosphate tribasic (742 mg, 3.5 mmol) in toluene (15 mL) and water (3 mL) was de-gassed and purged with argon and the reaction mixture was heated at 70° C. for 5 h. The mixture was cooled and partitioned between ethyl acetate and water. The layers were separated and the organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The resultant residue was purified by silica gel flash chromatography (20% ethyl acetate in cyclohexane) to afford the title compound as a pale yellow solid (396 mg, 57% yield). 1H NMR (400 MHz, DMSO-d6): δ 10.19 (s, 1H), 9.05 (s, 1H), 7.92 (d, J=3.1 Hz, 1H), 7.80 (d, J=8.2 Hz, 2H), 7.72 (d, J=7.9 Hz, 1H), 1.48 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309240B2
Source datasetuspto-grants-2016_04
ORD IDord-6a3d03b7b2cb4987849e6ea9de6c5d21
Source noteuspto-grants-2016_04