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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896533Generated: October 30, 2026

Sodium Carbonate → HCID 59198487, compound

https://huagongshe.com/reaction/1896533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
Reactanttrans-2-(4-Fluorophenyl)vinylboronic acidHCID 5706776—
Reactant7-Bromo-1-[(4-methoxybenzyl)amino][1]benzothieno[3,2-c]pyridine-4-carbonitrileHCID 59198465—
Catalystpalladium(II) acetateHCID 167845—
Solvent1-PropanolHCID 1031—
ProductHCID 59198487HCID 59198487—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspension of 7-bromo-1-[(4-methoxybenzyl)amino][1]benzothieno[3,2-c]pyridine-4-carbonitrile (Example 12, Step 9) in 1-propanol (0.1 M) was added [(E)-2-(4-fluorophenyl)vinyl]boronic acid (1.5 equiv), 2.0 M aqueous Na2CO3 solution (2.5 equiv), and a 3:1 mixture of Ph3P:Pd(OAc)2 (0.1 equiv). The mixture was degassed and then stirred at 100° C. for 2.5 h, and was then partitioned between EtOAc/THF and H2O. The organic layer was washed with H2O and brine, and was then dried (MgSO4), filtered, and evaporated. The crude material was purified by flash chromatography, eluting with 1:1 Et2O:hexanes. The product was stirred with 1:10 EtOAc:hexanes containing trace acetone to yield the title compound as a pale yellow solid after filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518964B2
Source datasetuspto-grants-2013_08
ORD IDord-be1583acaf064d7aabe6385f22142d36
Source noteuspto-grants-2013_08