HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930459Generated: October 28, 2026
Phosphorus oxychloride → Methyl 5-chloro-3-methylpyrazine-2-carboxylate
https://huagongshe.com/reaction/930459
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 3-(Methoxycarbonyl)-2-methylpyrazine 1-oxide | HCID 66665356 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 5-chloro-3-methylpyrazine-2-carboxylate | HCID 72218580 | 22% |
Reaction Steps
In a 1-L flask, the crude 3-(methoxycarbonyl)-2-methylpyrazine 1-oxide (step 2, 17.77 g, 106 mmol) was dissolved in DMF (300 mL). Neat phosphoryl trichloride (29.6 mL, 317 mmol) was added. The reaction mixture was heated to 100° C. After 1 h, the reaction mixture was concentrated to remove most of the DMF. The flask was cooled in an ice water bath, and 1 M aqueous Na2CO3 (300 mL) was added slowly, followed by 80% EtOAc-hexane (400 mL). The mixture was filtered through Celite. The resulting filtrate was partitioned and the aqueous phase was extracted further with 80% EtOAc-hexane (2×250 mL). The combined organic layers were dried over MgSO4 and concentrated. The material was purified through silica gel using 11% EtOAc-hexane to afford the title compound (4.29 g, 23 mmol, 22%). MS m/z=187 [M+H]+. Calculated for C7H7ClN2O2: 186. 1H NMR in CDCl3 δ: 8.51 (s, 1H), 4.01 (s, 3H), 2.86 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09296734B2 |
|---|
| Source dataset | uspto-grants-2016_03 |
|---|
| ORD ID | ord-3fbf27164ea04788ac40aaa21af8700c |
|---|
| Source note | uspto-grants-2016_03 |
|---|