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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389499Generated: October 26, 2026

Potassium Carbonate → ethyl {4-[7-amino-2-(isoquinolin-5-yl)furo[2,3-c]pyridin-4-yl]-1H-pyrazol-1-yl}acetate

https://huagongshe.com/reaction/389499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantIsoquinoline-5-boronic acidHCID 599474—
Reactantethyl[4-(7-amino-2-chlorofuro[2,3-c]pyridin-4-yl)-1H-pyrazol-1-yl]acetateHCID 101043349—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Productethyl {4-[7-amino-2-(isoquinolin-5-yl)furo[2,3-c]pyridin-4-yl]-1H-pyrazol-1-yl}acetateHCID 5337806741%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of isoquinoline-5-boronic acid (53.9 mg, 0.312 mmol) and ethyl[4-(7-amino-2-chlorofuro[2,3-c]pyridin-4-yl)-1H-pyrazol-1-yl]acetate (50.0 mg, 0.156 mol) in 1,4-dioxane (0.85 mL) and H2O (0.3 mL) was charged with potassium carbonate (32 mg, 0.23 mmol) and (1,1′-bis(diphenylphosphino)ferrocene)palladium dichloride (1 mg, 0.002 mmol) under an atmosphere of nitrogen. The mixture was heated in a microwave reactor at 100° C. for 40 min. Purification of the residue by flash chromatography (0 to 5% 7 N NH3/MeOH:EtOAc) afforded 27 mg (41%) of the title compound. 1H NMR (400 MHz, CD3OD) δ 9.36 (s, 1H), 8.57-8.63 (m, 1H), 8.52 (d, J=6.06 Hz, 1H), 8.37 (d, J=7.33 Hz, 1H), 8.27 (d, J=8.08 Hz, 1H), 8.18 (s, 1H), 7.98 (d, J=7.58 Hz, 2H), 7.85 (t, J=7.83 Hz, 1H), 7.55-7.62 (m, 1H), 7.53 (s, 1H), 4.28 (q, J=7.16 Hz, 2 H), 1.95 (s, 2H), 1.32 (t, 3H); MS (ESI): 415.16 [M+H]+; HPLC tR=0.94 min (TOF: polar—3 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378104B2
Source datasetuspto-grants-2013_02
ORD IDord-70bd4764c74c494ea25974bedc29e6fb
Source noteuspto-grants-2013_02