HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Bromo-4,5-dihydropyrido[4,3-b]thieno[2,3-d]oxepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4,5-Dihydropyrido[4,3-b]thieno[2,3-d]oxepine | HCID 57900199 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Bromo-4,5-dihydropyrido[4,3-b]thieno[2,3-d]oxepine | HCID 57900091 | 65.4% |
Reaction Steps
N-Bromosuccinimide (0.237 g, 1.33 mmol) in dimethylformamide (4 mL) was added dropwise to a solution of 4,5-dihydropyrido[4,3-b]thieno[2,3-d]oxepine (0.250 g, 1.23 mmol) in dimethylformamide (4 mL, 100 mmol) at 0° C. The reaction mixture was stirred for 18 hours at room temperature. The reaction mixture was mixed with 40 ml of water and extracted with 20 ml of ethylacetate twice. Combined organic extracts were washed with water and brine, and dried over MgSO4. The solvent was evaporated affording 2-bromo-4,5-dihydropyrido[4,3-b]thieno[2,3-d]oxepine (0.227 g, 63%). 1H NMR (500 MHz, CDCl3) 8.76 (s, 1H), 8.26 (d, J=5.4, 1H), 6.90 (d, J=5.5, 1H), 6.88 (s, 1H), 4.36 (t, J=4.7, 2H), 3.19 (t, J=4.8, 2H). MS (ESI+) 282.0
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846762B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-213476a895a04bf08c0233c3f51e62c8 |
| Source note | uspto-grants-2014_09 |