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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655056Generated: November 1, 2026

methyl 1H-indole-4-carboxylate → HCID 54402352, compound

https://huagongshe.com/reaction/1655056

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 1H-indole-4-carboxylateHCID 2733668—
Reactant2-(4-Chloromethylphenoxy)methylquinolineHCID 14774163—
ReactantHCID 178418573HCID 178418573—
SolventDimethylformamideHCID 6228—
SolventButyl etherHCID 8909—
ProductHCID 54402352HCID 54402352—

Reaction Steps

A solution of methyl magnesium bromide in n-butyl ether (1.0M, 10.3 ml) was added dropwise to a solution of methyl indole-4-carboxylate (1.5 g) in dry dimethylformamide (15 ml) stirred under an atmosphere of nitrogen at room temperature. The mixture was stirred at room temperature for 20 minutes then a solution of 4-(quinolin-2-ylmethoxy)benzyl chloride (Example 1a) (2.35 g) in dry dimethylformamide (10 ml) added dropwise. The mixture was stirred at room temperature overnight, concentrated in vacuo, diluted with ethyl acetate and washed with water and a saturated solution of ammonium chloride; the organic phase was dried, filtered and evaporated. The residue was purified by chromatography on flash silica, eluting with petroleum spirit 40°-60° C.--diethyl ether (1:1) to give the product as a white solid. A small quantity was crystallised from petroleum spirit 40°-60° C.--diethyl ether (1:1), m.p. 148°-150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05410061
Source datasetuspto-grants-1995_04
ORD IDord-f3847ded8c884b36895affb2a38109c1
Source noteuspto-grants-1995_04