HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Azido-7-fluoro-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3-iodo-7-fluoro-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one | HCID 54199051 | — |
| Reactant | HCID 178484365 | HCID 178484365 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Azido-7-fluoro-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one | HCID 53862901 | 90.9% |
Reaction Steps
101 mg (0.33 mmol) of 3-iodo-7-fluoro-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one (Step B) was dissolved in 8.3 mL of methylene chloride and 105 mg (0.66 mmol, 2 eq) of tetramethylguanidinium azide was added. The mixture was stirred at room temperature for 16 hours then water was added and the layers allowed to separate. The organic layer was removed, washed with water and brine, then dried over magnesium sulfate, filtered and solvents removed under vacuum to afford 66 mg (0.30 mmol, 90%) of the product. 1H NMR (200MHz, CDCl3): 2.28 (m,1H), 2.45 (m,1H), 2.73 (m,1H), 2.93 (m,1H), 3.86 (dd:8,11 Hz;1H), 7.0 (m,3H), 8.15 (br s,1H). FAB-MS: calculated for C10H9FN4O 220: found 221 (M+H,100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05310737 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-c777f54b6ad44a8a8da50a4e9d93f728 |
| Source note | uspto-grants-1994_05 |