HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509440Generated: November 3, 2026
Hydrogen Bromide → HCID 178523849, compound
https://huagongshe.com/reaction/509440
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 71144214 | HCID 71144214 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178523849 | HCID 178523849 | — |
Reaction Steps
To a solution of 30% HBr in AcOH (10 mL, Spectrochem, India) was added (S)—N-((3-fluoro-4-(trifluoromethoxy)phenyl)(3-fluoropyridin-2-yl)methyl)-4-methoxy-5-nitropicolinamide (1 g, 0.002 mol), and the resulting reaction mixture was stirred for 12 h at 90° C. The reaction progress was monitored by TLC (50% EtOAc in petroleum ether). After completion of the reaction, the reaction mixture was concentrated and neutralized with sat'd NaHCO3 solution (pH˜7-7.5) and the aqueous solution was extracted with EtOAc (3×10 mL). The combined organic layers were dried over anhydrous sodium sulfate, and concentrated to afford the title compound as a pale yellow solid. 1H NMR (DMSO-d6) δ: 9.84 (d, J=7.5 Hz, 1H), 8.77 (s, 1H), 8.53 (d, J=4.5 Hz, 1H), 7.83-7.70 (m, 1H), 7.57-7.49 (m, 3H), 7.38-7.31 (m, 2H), 6.56 (d, J=7.5 Hz, 1H). MS (ESI, positive ion) m/z: 471.4 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09096527B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-4ab5c62a81f84df4bae5f88c3c8f318e |
|---|
| Source note | uspto-grants-2015_08 |
|---|