HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7076Generated: October 28, 2026
Formic Acid → N-[3-(4-tert-butylcyclohexan-1-yl)phenyl]-4-[2-(N-formylamino)ethoxy]-3-methoxyphenylacetamide
https://huagongshe.com/reaction/7076
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-(2-aminoethoxy)-N-[3-(4-tert-butylcyclohexan-1-yl)phenyl]-3-methoxyphenylacetamide | HCID 22019602 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[3-(4-tert-butylcyclohexan-1-yl)phenyl]-4-[2-(N-formylamino)ethoxy]-3-methoxyphenylacetamide | HCID 22019592 | 75.2% |
Reaction Steps
Formic acid (30 mg) is slowly added to acetic anhydride (75 mg), and the mixture is heated with stirring at 60° C. for 2 hours. To the mixture is added dry tetrahydrofuran (0.2 ml), and further added 4-(2-aminoethoxy)-N-[3-(4-tert-butylcyclohexan-1-yl)phenyl]-3-methoxyphenylacetamide (100 mg) obtained in Example 62 at −20° C. The mixture is stirred at room temperature for 3 hours. The solvent is evaporated under reduced pressure, and the residue is purified by silica gel column chromatography (eluent: gradient from 0% to 100% hexane/ethyl acetate) to give the desired compound (80 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07084176B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-7a9766c478ba4aec9949a59023cce479 |
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| Source note | uspto-grants-2006_08 |
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