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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263727Generated: November 2, 2026

Methyl iodide → HCID 69659266, compound

https://huagongshe.com/reaction/1263727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTetrahydrofuranHCID 8028—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(6-Amino-2-benzofuran-1(3H)-ylidene)-1,3-dihydro-2H-indol-2-oneHCID 69659199—
CatalystSilver(I) trifluoromethanesulfonateHCID 76223—
ProductHCID 69659266HCID 69659266—
ProductHCID 69659761HCID 69659761—

Reaction Steps

To a solution of 3-(6-Amino-3H-isobenzofuran-1-ylidene)-1,3-dihydro-indol-2-one (50.0 mg, 0.189 mmol) and N,N-diisopropylethylamine (65.8 μL, 0.378 mmol) in 2.0 mL THF was added iodomethane (12.9 μL, 0.208 mmol). After stirring at room temperature for 21 h, silver triflate (53.4 mg, 0.208 mmol) was added and the mixture heated at 45° C. for 16 h. The mixture was partitioned between EtOAc and saturated NaHCO3 and the organic separated. The organic layer was washed with H2O, brine and then dried with Na2SO4. The solution was evaporated in vacuo and the residue purified by chromatography (silica gel, 2% MeOH/CHCl3) to give 3-(6-Dimethylamino-3H-isobenzofuran-1-ylidene)-1,3-dihydro-indol-2-one (3.6 mg) as a yellow solid and 3-(6-Methylamino-3H-isobenzofuran-1-ylidene)-1,3-dihydro-indol-2-one (6.3 mg) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541504B1
Source datasetuspto-grants-2003_04
ORD IDord-b2038ba7c3884d1682805462375e3104
Source noteuspto-grants-2003_04