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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428678Generated: October 30, 2026

2,3-Dimethoxybenzaldehyde → HCID 10224610, compound

https://huagongshe.com/reaction/428678

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DimethoxybenzaldehydeHCID 66581—
ReactantHCID 14037720HCID 14037720—
Reactant(Z)-4-bromo-1,3-dihydro-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-2H-indol-2-oneHCID 18359254—
ReactantHCID 178462451HCID 178462451—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 10224610HCID 10224610—

Reaction Steps

Using Method D above, 3-(2,3-dimethoxyphenyl)-3-hydroxy-1-propyne (132 mg, 0.69 mmol) (prepared by the addition of ethynylmagnesium chloride (Aldrich) to 2,3-dimethoxybenzaldehyde (Aldrich) according to Method A above) was coupled to (Z)-4-bromo-1,3-dihydro-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-2H-indol-2-one (Starting Material 1) (98 mg, 0.31 mmol) using (Ph3P)2PdCl2 (38 mg) (Aldrich) and CuI (17 mg) (Aldrich) as catalyst in DMF (3 mL) and Et3N (3 mL) as solvent at 70° C. for 17 h, yielding rac-(Z)-1,3-dihydro-4-[3-(2,3-dimethoxyphenyl)-3-hydroxy-1-propynyl]-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-2H-indol-2-one. (Yield 98 mg, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313310B1
Source datasetuspto-grants-2001_11
ORD IDord-acb533db8fb4460c94625b7f86cf8f5f
Source noteuspto-grants-2001_11