HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075455Generated: November 1, 2026
Methoxyacetic Acid → HCID 67090436, compound
https://huagongshe.com/reaction/2075455
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methoxyacetic Acid | HCID 12251 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | HCID 67089898 | HCID 67089898 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67090436 | HCID 67090436 | 39% |
Reaction Steps
A solution of methoxyacetic acid (0.019 mL, 0.24 mmol) in THF (5.0 mL) was added with Compound 95 (0.10 g, 0.29 mmol), 1-hydroxybenzotriazole monohydrate (52 mg, 0.337 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (69 mg, 0.36 mmol), followed by stirring at 60° C. for 1 hour. The reaction mixture was added with ethyl acetate and saturated aqueous sodium hydrogencarbonate solution (4.0 mL) and was extracted. The organic layer was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/methanol=10/1), and the product was added with ethyl acetate, then precipitate was collected by filtration to obtain Compound 100 (39 mg, 39%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07919517B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-dbc5833df785429d8c1431dfae195ad8 |
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| Source note | uspto-grants-2011_04 |
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