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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methyl-1H-indole-3-carbaldehyde | HCID 87894 | — |
| Reactant | Iodo benzene diacetate | HCID 12217721 | — |
| Reactant | Methyl (4-amino-2-fluoro-3-hydroxyphenyl)acetate | HCID 17859032 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 58779044 | HCID 58779044 | 50.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157487B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-99c7543ef46a426badce607a261086ba |
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| Source note | uspto-grants-2007_01 |
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