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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372757Generated: November 3, 2026

1-Methyl-1H-indole-3-carbaldehyde → HCID 58779044, compound

https://huagongshe.com/reaction/1372757

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-1H-indole-3-carbaldehydeHCID 87894—
ReactantIodo benzene diacetateHCID 12217721—
ReactantMethyl (4-amino-2-fluoro-3-hydroxyphenyl)acetateHCID 17859032—
SolventMethanolHCID 887—
ProductHCID 58779044HCID 5877904450.8%

Reaction Steps

In methanol (50 ml), 3-formyl-1-methylindole (796 mg, 5.0 mmol), methyl (4-amino-2-fluoro-3-hydroxyphenyl)acetate (1.0 g, 5.0 mmol) and Molecular Sieves 4A (10 g) were stirred at room temperature for 5 hours and then, at 70° C. for 3 hours. The reaction mixture was cooled to room temperature and iodobenzene diacetate (5.0 mmol) was added thereto. After stirring at room temperature for 14 hours, the reaction mixture was distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from n-hexane/ethyl acetate (3/1) eluate fractions, methyl 7-fluoro-2-(1-methyl-3-indolyl)-6-benzoxazolylacetate (860 mg, including impurities) was obtained as a pale brown solid. The compound was provided for the subsequent reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-99c7543ef46a426badce607a261086ba
Source noteuspto-grants-2007_01