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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366682Generated: October 26, 2026

(Prop-2-yn-1-yl)urea → (z)-[3-[5-Fluoro-2,3-dihydro-3-[(4-methyl-1h-imidazol-5-yl)methylene]-2-oxo-1h-indol-4-yl]-2-propynyl]urea

https://huagongshe.com/reaction/366682

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Prop-2-yn-1-yl)ureaHCID 2777182—
ReactantHCID 178433242HCID 178433242—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product(z)-[3-[5-Fluoro-2,3-dihydro-3-[(4-methyl-1h-imidazol-5-yl)methylene]-2-oxo-1h-indol-4-yl]-2-propynyl]ureaHCID 178433241—

Reaction Steps

Using Method C above, 2-propynylurea (50 mg, 0.51 mmol) (see below) was coupled with (Z)-1,3-dihydro-5-fluoro-4-iodo-3-[(4-methyl-1H-imidazol-5-yl)methylene]-2H-indol-2-one (Starting Material 3 supra) (75 mg, 0.203 mmol) using (Ph3P)4Pd (23.5 mg) and Cul (4 mg) as catalyst in DMF (3 mL) and Et3N (3 mL) as solvent at 80° C. for 18 h to give (Z)-[3-[5-fluoro-2,3-dihydro-3-[(4-methyl-1H-imidazol-5-yl)methylene]-2-oxo-1H-indol-4-yl]-2-propynyl]urea. (Yield 11 mg, 16%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130239
Source datasetuspto-grants-2000_10
ORD IDord-24cb2a7492bb4e7fac14c31fd60dfead
Source noteuspto-grants-2000_10