HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207065Generated: October 31, 2026
Potassium Iodide → Ethyl 2-((4-((2-amino-4-(mesitylsulfonyloxy)-6-methylpyrimidin-5-yl)methyl)-3-methoxybenzyl)(ethyl)amino)acetate
https://huagongshe.com/reaction/2207065
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Ethyl 2-(ethylamino)acetate | HCID 12591597 | — |
| Reactant | Potassium dicarbonate | HCID 86587255 | — |
| Reactant | 2-Amino-5-(4-(chloromethyl)-2-methoxybenzyl)-6-methylpyrimidin-4-yl 2,4,6-trimethylbenzenesulfonate | HCID 87945075 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 2-((4-((2-amino-4-(mesitylsulfonyloxy)-6-methylpyrimidin-5-yl)methyl)-3-methoxybenzyl)(ethyl)amino)acetate | HCID 117992606 | — |
Reaction Steps
The product from step (vi) (390 mg) was added to the mixture of potassium dicarbonate (410 mg), potassium iodide (49 mg) and the crude product from step (v) in acetonitrile (5 mL). After the mixture was stirred at 70° C. for 4 h, the reaction mixture was cooled to RT, filtered, and concentrated under reduced pressure. The residue was purified by flash column chromatography to afford the sub-title compound (490 mg) as a colourless amorphous solid; 1H NMR (300 MHz, CDCl3); 6.91 (2H, s), 6.87 (1H, s), 6.72 (2H, s), 4.65 (2H, br s), 4.14 (2H, q), 3.82-3.79 (5H, m), 3.70 (2H, s), 3.28 (2H, s), 2.67 (2H, q), 2.56 (6H, s), 2.28 (3H, s), 2.23 (3H, s), 1.25 (3H, t), 1.07 (3H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376398B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-d1a4c0816a844a138f9830cd1f043d88 |
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| Source note | uspto-grants-2016_06 |
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