HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 22992850, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-piperidin-1-ylpyridine | HCID 817759 | — |
| Reactant | HCID 22992851 | HCID 22992851 | — |
| Product | HCID 22992850 | HCID 22992850 | 93% |
Reaction Steps
169 mg of the 4-(4-chlorobutyl)-3,8-dichloro-4,5-dihydro-1,4-benzoxazepin-5-one synthesized by the method of Example 17 described in International Publication WO96/24594 was dissolved in 3 ml of dimethylformamide, then 129 mg (1.5 equivalents) of 1-(2-pyridyl)piperadine, 158 mg (2 equivalents) of sodium iodide, and 106 mg (2 equivalents) of triethylamine were added and the resultant mixture agitated at 80° C. for 6 hours. This was treated and refined in the same way as Example 13 to obtain 219 mg of the above-referenced compound (yield 93%). Note that the dichloride was obtained by making a dichloride by an ordinary method, then recrystallizing from a mixed solvent of methanol, chloroform, and ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06114522 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-ae38826c430f4c7cbfd7c1128a190d27 |
| Source note | uspto-grants-2000_09 |