HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098268Generated: November 2, 2026
Potassium Sodium Tartrate → HCID 57504565, compound
https://huagongshe.com/reaction/1098268
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Sodium Tartrate | HCID 9357 | — |
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 66813606 | HCID 66813606 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57504565 | HCID 57504565 | 84.5% |
Reaction Steps
Trimethylaluminium (8.31 mL, 16.62 mmol) was added to pyridin-2-amine (1.360 g, 14.45 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-(azetidin-1-yl)-2-hydroxypropanoate (Intermediate BC2) (2.3 g, 14.45 mmol) in toluene (10 mL) and THF (5 mL) was added and the resulting solution was allowed to warm to room temperature and then heated at 60° C. for 8 hours. The reaction cooled and 20% Rochelle salt (50 mL) added followed by EtOAc (50 mL) and the mixture stirred at ambient temperature overnight. The organic phase separated and the aqueous phase re-extracted with EtOAc (2×50 mL). The organic phases were combined, dried (MgSO4) and evaporated to afford the product (2.7 g) which was used without further purification.
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-5e368e1fee17422b9fa49f1eb0427cac |
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| Source note | uspto-grants-2012_03 |
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