HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 131721977, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(Piperidin-1-yl)pyrimidine | HCID 11446518 | — |
| Reactant | HCID 18328146 | HCID 18328146 | — |
| Product | HCID 131721977 | HCID 131721977 | 83% |
Reaction Steps
129 mg of the 3-chloro-4-(4-chlorobutyl)-4,5-dihydro-7-methyl-1,4-benzoxazepin-5-one synthesized by the method of Example 19 described in International Publication WO96/24594 was dissolved in 2 ml of dimethylformamide, then 106 mg (1.5 equivalents) of 1-(2-pyrimidinyl)piperadine, 129 mg (2 equivalents) of sodium iodide, and 87 mg (2 equivalents) of triethylamine were added and the resultant mixture agitated at 90° C. for 7 hours. This was then treated and purified in the same way as Example 13 to obtain 152 mg of the above-referenced compound (yield 83%). Note that the dichloride was obtained by making a dichloride by an ordinary method, then recrystallizing from ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06114522 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-d856a144f3a340ed861e81022b6ae944 |
| Source note | uspto-grants-2000_09 |