HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530540Generated: November 4, 2026
Dimethylformamide → 10-Bromo-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamide
https://huagongshe.com/reaction/1530540
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Hexamethyldisilazane | HCID 13838 | — |
| Reactant | 10-Bromo-2-iodo-5,6-dihydrobenzo[F]imidazo[1,2-D][1,4]oxazepine | HCID 58204407 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Product | 10-Bromo-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxamide | HCID 68312883 | 95% |
Reaction Steps
To a solution of 13-bromo-4-iodo-9-oxa-3,6-diazatricyclo[8.4.0.02,6]tetradeca1(14),2,4,10,12-pentaene (5.0 g, 0.013 mol) in DMF (50 mL) was added hexamethyldisilazane (16 mL, 0.077 mol) and Pd(PPh3)2Cl2 (0.45 g, 0.639 mmol). After being purged with CO three times, the mixture was heated at 70° C. for 3 h. After removal of the solvent, water (100 mL) was added. The solid was collected by filtration, washed with water, and dried in vacuo to afford the title compound (3.8 g, 95% yield) as a yellow solid. LCMS m/z [M+H]+ 309.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090628B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-cd38935e151048df9bcdf0e499e05ff0 |
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| Source note | uspto-grants-2015_07 |
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