HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 8-Bromo-1,2,3,4-tetrahydronapthyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1,2,3,4-Tetrahydro-1,8-naphthyridine | HCID 13047367 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 8-Bromo-1,2,3,4-tetrahydronapthyridine | HCID 86584174 | — |
Reaction Steps
To a solution of 0.6730 g (5.02 mmol) 32 in 20 mL glacial acetic acid was added 1.0701 g (6.01 mmol) N-bromosuccinimide. After 16 h at 65° C., the reaction mixture was cooled to room temperature and poured onto 50 mL ice water. This was brought to pH 11 with K2CO3 and extracted with 4×100 mL CHCl3. The combined CHCl3 extracts were washed with 100 mL brine, dried over Na2SO4, filtered and concentrated in vacuo. Purification by flash chromatography (50×115 mm silica gel, linear gradient 2-5% (10% NH4H:MeOH):CH2Cl2) yielded 33. 1H NMR (CDCl3, 400 MHz) δ 8.175 (s, 1H, ArH); 7.877 (s, 1H, ArH); 3.458-3.423 (m, 2H, CH2); 2.725 (t, 2H, J=6.26 Hz, CH2); 1.970-1.911 (m, 2H, CH2); MS (Electrospray): m/z 212.9, 214.8 (M+H, 79Br, 81Br).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06534510B2 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-f0057b796b874921a888db3bf6e4eb38 |
| Source note | uspto-grants-2003_03 |