HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646762Generated: November 1, 2026
Carbon tetrabromide → HCID 68651040, compound
https://huagongshe.com/reaction/646762
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 68650646 | HCID 68650646 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68651040 | HCID 68651040 | 77% |
Reaction Steps
To a solution of 3-amino-N-ethyl-6-[3-(hydroxymethyl)phenyl]pyrazine-2-carboxamide (566.1 mg, 1.0 eq) in dichloromethane (20 mL) were added carbon tetrabromide (749.8 mg, 1.1 eq), triphenylphosphine (600 mg, 1.1 eq) at ambient temperature. After being stirred for 7 h, the reaction mixture was partitioned with dichloromethane (10 mL×3), washed with brine. The organic layer was combined and dried over anhydrous magnesium sulfate. Filteration and concentration in vacuo gave a crude product. Purification by column chromatography afforded the 3-amino-6-[3-(bromomethyl)phenyl]-N-ethylpyrazine-2-carboxamide (534 mg, 77% yield): 1H NMR (400 MHz, DMSO-d6): δ 8.87 (m, 2H), 8.84 (s, 2H), 8.23 (m, 1H), 7.61 (bs, 1H), 7.45 (m, 1H), 4.77 (s, 2H), 3.38 (m, 2H), 1.16 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07704995B2 |
|---|
| Source dataset | uspto-grants-2010_04 |
|---|
| ORD ID | ord-eb11924fd29c45b8a2fd0895147f8fdc |
|---|
| Source note | uspto-grants-2010_04 |
|---|