HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38754Generated: October 25, 2026
Methyl iodide → Alanine, N-[4-(aminocarbonyl)-3-fluorophenyl]-2-methyl-, methyl ester
https://huagongshe.com/reaction/38754
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-((4-Carbamoyl-3-fluorophenyl)amino)-2-methylpropanoic acid | HCID 66617902 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Alanine, N-[4-(aminocarbonyl)-3-fluorophenyl]-2-methyl-, methyl ester | HCID 66617687 | — |
Reaction Steps
A solution of 2-(4-carbamoyl-3-fluorophenylamino)-2-methylpropanoic acid and K2CO3 (1.5 equivalents) in DMF (10 fold) was stirred at RT for 10 min. MeI (1.5 equivalents) was added and the reaction mixture was heated at 55-60° C. for 2 h. The solvent was removed under reduced pressure and the reaction mixture was poured in water, extracted with ethyl acetate (100 mL×2), dried over Na2SO4, concentrated and purified by column chromatography. 1H NMR (CDCl3, Freebase): δ (ppm) 7.9 (t, 1H), 6.5 (bs, 1H), 6.4 (d, 1H), 6.2 (d, 1H), 5.6 (bs, 1H), 4.6 (bs, 1H), 3.75 (s, 3H), 1.6 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524755B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-271f30e301a24d199343b3db95c1ef10 |
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| Source note | uspto-grants-2013_09 |
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