HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454901Generated: October 29, 2026
Dimethyl Sulfoxide → Benzyl 3-(3-chloropyrazin-2-yloxy)azetidine-1-carboxylate
https://huagongshe.com/reaction/454901
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | 2,3-Dichloropyrazine | HCID 78575 | — |
| Reactant | Benzyl 3-hydroxyazetidine-1-carboxylate | HCID 10081755 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzyl 3-(3-chloropyrazin-2-yloxy)azetidine-1-carboxylate | HCID 58547798 | 61.6% |
Reaction Steps
To a solution of 3-hydroxy-azetidine-1-carboxylic acid benzyl ester (5.19 g, 27.4 mmol, purchased from Ace Synthesis), 2,3-dichloropyrazine (4.116 g, 27.6 mmol, Oakwood) and DMSO (40 mL) was added sodium tert-butoxide (2.64 g, 27.4 mmol) in three portions. The solution was allowed to stir at room temperature. After 2 hours, the reaction was poured into water (200 mL) and the aqueous solution was extracted with ether (3×50 mL). The combined ether layers were washed with water (50 mL), brine (50 mL), and then concentrated in vacuo. The crude product was adsorbed onto a plug of silica gel and chromatographed through a Redi-Sep® pre-packed silica gel column (80 g), eluting with 0% to 20% EtOAc in hexane, to provide benzyl 3-(3-chloropyrazin-2-yloxy)azetidine-1-carboxylate (5.4 g, 61.6% yield), as a yellow oil. MS (ESI) m/z 320.1 (MH+). ICSO (uM): 1.33.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08497265B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
|---|
| ORD ID | ord-31c543a8954e4b1bb8fceb88f63eecde |
|---|
| Source note | uspto-grants-2013_07 |
|---|