HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843717Generated: November 3, 2026
Triethylamine → Methyl 3-[2-({4-[(2-methoxypyridin-4-yl)oxy]-2-(methylamino)phenyl}amino)-2-oxoethoxy]benzoate
https://huagongshe.com/reaction/1843717
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | [3-(Methoxycarbonyl)phenoxy]acetic acid | HCID 13816150 | — |
| Reactant | 4-[(2-Methoxypyridin-4-yl)oxy]-N2-methylbenzene-1,2-diamine | HCID 66705864 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-[2-({4-[(2-methoxypyridin-4-yl)oxy]-2-(methylamino)phenyl}amino)-2-oxoethoxy]benzoate | HCID 66705881 | 78% |
Reaction Steps
Pivaloyl chloride (1.74 mL, 14.2 mmol) was added dropwise to a solution of [3-(methoxycarbonyl)phenoxy]acetic acid produced in Example (1c) (3.27 g, 15.6 mmol) and triethylamine (1.97 mL, 14.2 mmol) in dichloromethane (40 mL) in a nitrogen atmosphere at 0° C. After one hour, a solution of 4-[(2-methoxypyridin-4-yl)oxy]-N2-methylbenzene-1,2-diamine produced in Example (16d) (3.46 g, 14.2 mmol) and triethylamine (1.97 mL, 14.2 mmol) in dichloromethane (40 mL) was added dropwise at 0° C., and the mixture was stirred at room temperature for two hours. The reaction mixture was concentrated under reduced pressure. Then, the residue was purified by silica gel chromatography (ethyl acetate) to obtain the title compound (4.81 g, 78%) as a pale brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946264B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-8c78410083224c04b8f3f00b1be56ed0 |
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| Source note | uspto-grants-2015_02 |
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