HuagongsheHuagongshe Chemistry Print Report · For research reference only
8-chlorodibenz[b,f][1,4]oxazepin-10(11H)carbonyl chloride → HCID 86748368, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 8-chlorodibenz[b,f][1,4]oxazepin-10(11H)carbonyl chloride | HCID 14975983 | — |
| Reactant | HCID 14976003 | HCID 14976003 | — |
| Reactant | HCID 86748367 | HCID 86748367 | — |
| Product | HCID 86748368 | HCID 86748368 | — |
Reaction Steps
8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[2,2-difluoro-3-hydroxyl-1-oxo-3-(2-thienyl)propyl]hydrazide (27) was prepared in the same manner as 8-chlorodibenz[b,f][1,4]-oxazepine-10(11H)-carboxylic acid, 2-[2,2-difluoro-3-hydroxy-1-oxo-3-(2-pyridinyl)propyl]hydrazide (11), as described above in Example 11, on a 0.9 mmol scale from α,α-difluoro-β-hydroxy-2-thiophenepropanoic acid, hydrazide (26), prepared as described above in Example 26, and 8-chlorodibenz[b,f][1,4]-oxazepine-10(11H)-carbonyl chloride (2), prepared as described above in Example 2, to yield 0.15 g (39%) of product. Analysis calculated for C21H16N3O4SF2Cl. H2O (M.W. 497.91): C, 50.66; H, 3.64; N, 8.44. Found: C, 50.89; H, 3.33; N, 8.24.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05576315 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-075b90ab65ea4ef481e899440cca441d |
| Source note | uspto-grants-1996_11 |