HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Pyridinemethanamine → HCID 131719084, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Pyridinemethanamine | HCID 19509 | — |
| Reactant | 8-chlorodibenz[b,f][1,4]oxazepin-10(11H)carbonyl chloride | HCID 14975983 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 131719084 | HCID 131719084 | — |
Reaction Steps
By the method described in Example 18, the title compound of Example 2 in CH2Cl 2 with molecular sieves #5A and Et3N was reacted with 2-(aminomethyl)pyridine to generate the free base of the title product. This material was converted to the title compound by the method described in Example 40.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05441950 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-dce50d55dd6848c5830488b7a8232bb8 |
| Source note | uspto-grants-1995_08 |