HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787708Generated: October 25, 2026
2,6-Diaminopyridine → N-(6-Amino-pyridin-2-yl)-2-(2-methoxy-ethoxy)-acetamide
https://huagongshe.com/reaction/1787708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Diaminopyridine | HCID 8861 | — |
| Reactant | (2-Methoxyethoxy)acetic acid | HCID 27642 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | N-(6-Amino-pyridin-2-yl)-2-(2-methoxy-ethoxy)-acetamide | HCID 57600508 | — |
Reaction Steps
4.9 ml of (2-methoxyethoxy)-acetic acid is dissolved in 500 ml of tetrahydrofuran. 9.7 ml of triethylamine and 5.6 ml of isobutyl chloroformate are added at 0° C., and it is stirred for 30 minutes at 0° C. 3.96 g of 2,6-diaminopyridine is added, and it is stirred for another 4 hours at room temperature. The reaction mixture is mixed with semi-saturated sodium bicarbonate solution and extracted with ethyl acetate. The organic solution is washed with saturated sodium chloride solution, dried on sodium sulfate, concentrated by evaporation, and after purification by chromatography on silica gel, 5.04 g of the title compound is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07511059B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-1dda6433de5b4aab9845db9fde330951 |
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| Source note | uspto-grants-2009_03 |
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