HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dibromoethane → Methyl 5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-10-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | HCID 135742047 | HCID 135742047 | — |
| Product | Methyl 5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-10-carboxylate | HCID 58204321 | 76% |
Reaction Steps
Following the procedure in Example 17, methyl 4-hydroxy-3-(1H-imidazol-2-yl)benzoate reacted with 1,2-dibromoethane to give methyl 5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-10-carboxylate. Yield 76%. MS(ESI+): 245.0. 1H NMR (400 MHz, CDCl3) δ 9.21 (d, J=2.2, 1H), 7.91 (dd, J=8.6, 2.2, 1H), 7.20 (t, J=4.8, 1H), 7.05 (d, J=8.6, 1H), 7.00 (d, J=0.8, 1H), 4.53-4.48 (m, 2H), 4.43-4.39 (m, 2H), 3.91 (d, J=5.9, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09198918B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-ef1cb292e92b465d9917d003be94c81c |
| Source note | uspto-grants-2015_12 |