HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → isopropyl 7-bromo-3-oxo-3,4-dihydroquinoxaline-1(2H)-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Isopropyl chloroformate | HCID 7917 | — |
| Reactant | 6-Bromo-1,2-dihydroquinoxalin-2-one | HCID 12686394 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | isopropyl 7-bromo-3-oxo-3,4-dihydroquinoxaline-1(2H)-carboxylate | HCID 18464405 | 97% |
Reaction Steps
To a solution of 7-bromo-3-oxo-3,4-dihydroquinoxaline (6.8 g, 30 mmol) in pyridine (50 ml) was added a solution of isopropyl chloroformate in toluene (35 ml, 1M, 35 mmol) over 30 minutes. The mixture was triturated with water/chloroform, the organic layer was separated, washed with brine, dried over magnesium sulfate, and evaporated to obtain crude isopropyl 7-bromo-3-oxo-3,4-dihydroquinoxaline-1(2H)-carboxylate(9.3 g, 97%). A sample was recrystallized from ethanol: m.p. 159-161° C. 1H-NMR (DMSO-d6) δ 1.25 (d, J=6.2 Hz, 6H), 4.25 (s, 2H), 4.90 (Sep, J=6.2 Hz, 1H), 6.89 (d, J=8.6 Hz, 1H), 7.27 (dd, J=9.1, 2.1 Hz, 1H), 7.74 (s, 1H), 12.51 (s, 1H), MS (ESI) m/z 330/332 (M+NH4)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06794373B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-605b71f5872e4b45a9bc43b1a0dfaa1d |
| Source note | uspto-grants-2004_09 |