HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708580Generated: October 27, 2026
Sodium Carbonate → Methyl (s)-2-((tert-butoxycarbonyl)amino)-3-(4-(2,3-dimethylpyridin-4-yl)phenyl)propanoate
https://huagongshe.com/reaction/708580
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | methyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]propanoate | HCID 10949509 | — |
| Reactant | 4-Bromo-2,3-dimethylpyridine | HCID 22317941 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl (s)-2-((tert-butoxycarbonyl)amino)-3-(4-(2,3-dimethylpyridin-4-yl)phenyl)propanoate | HCID 66719739 | 57.7% |
Reaction Steps
Suzuki Coupling. To a mixture of (S)-2-tert-butoxycarbonylamino-3-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-propionic acid methyl ester (8.22 g) in 140 mL toluene and 40 mL water was added 4-bromo-2,3-dimethyl-pyridine (6.77 g), Na2CO3 (7.5 g), and Pd(PPh3)4. The mixture was purged with nitrogen and stirred under nitrogen at 80° C. for 18 h. The mixture was then cooled to rt and poured into water-EtOAc. The organic layer was washed with water and saturated brine, dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by column chromatography (hexanes-EtOAc) to provide (S)-2-tert-butoxycarbonylamino-3-[4-(2,3-dimethyl-pyridin-4-yl)-phenyl]-propionic acid methyl ester (4.5 g). LCMS (m/z) 386.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09175003B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-9cd7b194c5ac4a09aeb486f8f43fc1e3 |
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| Source note | uspto-grants-2015_11 |
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