HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098273Generated: October 26, 2026
Potassium Sodium Tartrate → (S)-3-(3-(tert-butyldimethylsilyloxy)azetidin-1-yl)-2-hydroxy-N-(pyridin-2-yl)propanamide
https://huagongshe.com/reaction/1098273
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Sodium Tartrate | HCID 9357 | — |
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | (S)-methyl 3-(3-(tert-butyldimethylsilyloxy)azetidin-1-yl)-2-hydroxypropanoate | HCID 57504648 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (S)-3-(3-(tert-butyldimethylsilyloxy)azetidin-1-yl)-2-hydroxy-N-(pyridin-2-yl)propanamide | HCID 57504737 | 85.7% |
Reaction Steps
Trimethylaluminium (2.384 mL, 4.77 mmol) was added to pyridin-2-amine (0.390 g, 4.15 mmol) in toluene (30 mL) cooled to 0° C. under nitrogen. The resulting solution was stirred at 0° C. for 10 minutes. (S)-methyl 3-(3-(tert-butyldimethylsilyloxy)azetidin-1-yl)-2-hydroxypropanoate (Intermediate AD3) (1.2 g, 4.15 mmol) in toluene (10 mL) was added and the reaction was allowed to warm to room temperature and then heated at 80° C. for 4 hours. The reaction mixture was cooled, 20% Rochelle salt in water (75 mL) added and stirred for 2 hours. The mixture was extracted with ethyl acetate (2×5 mL) and the combined organic extracts washed with water (50 mL) and brine (50 mL), dried (MgSO4), filtered and evaporated. The crude product was purified by flash silica chromatography, elution gradient 0 to 10% MeOH in EtOAc to afford the product (1.25 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143263B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-c149492c26af4595b3a15d8509cbd22b |
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| Source note | uspto-grants-2012_03 |
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