Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623483Generated: November 3, 2026

Triphenylphosphine → HCID 67036257, compound

https://huagongshe.com/reaction/1623483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantCesium fluorideHCID 25953—
Reactant4-Chlorophenylboronic acidHCID 74299—
ReactantHCID 67036178HCID 67036178—
Catalystpalladium(II) acetateHCID 167845—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67036257HCID 6703625744.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 3-{[(2-iodo-phenyl)-(4-methyl-pent-2-ynoyl)-amino]-methyl}-benzoic acid methyl ester (0.93 g, 2.02 mmol), 4-chlorophenylboronic acid (0.63 g, 4.04 mmol), triphenylphosphine (53 mg, 0.202 mmol), palladium acetate (23 mg, 0.10 mmol) and cesium fluoride (0.92 g, 6.06 mmol) in THF (15 ml) was stirred for 3 hours at 60° C. After removal of solvent, the residue was purified by flash chromatography, eluting with ethyl acetate/hexane=1:5 to afford the product 3-{3-[1-(4-chloro-phenyl)-2-methyl-propylidene]-2-oxo-2,3-dihydro-indol-1-ylmethyl}-benzoic acid methyl ester (0.40 g, 44%) as a yellow solid. MS calcd. for C27H24ClNO3 445.5, obsd. (ESI+) [(M+H)+] 446.0. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.10 (d, J=6.82 Hz, 6H) 3.91 (s, 3H) 4.99 (dt, J=13.71, 6.92 Hz, 1H) 5.06 (s, 2H) 5.73 (d, J=7.58 Hz, 1H) 6.62 (t, J=7.71 Hz, 1H) 6.73 (d, J=7.83 Hz, 1H) 7.05 (t, J=7.71 Hz, 1H) 7.19 (d, J=8.34 Hz, 2H) 7.46 (t, J=7.83 Hz, 1H) 7.55 (d, J=8.08 Hz, 3H) 7.94 (d, J=7.58 Hz, 1H) 8.02 (s, 1H) MS calcd. for C27H24ClNO3 445.5, obsd. (ESI+) [(M+H)+] 446.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778973B2
Source datasetuspto-grants-2014_07
ORD IDord-fc492f49208a466ba4649c79aaa10620
Source noteuspto-grants-2014_07