HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646892Generated: October 25, 2026
Triethyl phosphite → 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[(diethoxyphosphinyl)acetyl]hydrazide
https://huagongshe.com/reaction/1646892
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | 2-Naphthylalanine | HCID 185915 | — |
| Reactant | 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)carboxylic acid | HCID 21983467 | — |
| Reactant | 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-(bromoacetyl) hydrazide | HCID 86746505 | — |
| Catalyst | Sodium Iodide | HCID 5238 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[(diethoxyphosphinyl)acetyl]hydrazide | HCID 9956259 | 83% |
Reaction Steps
To a stirring solution of 2.57 g (6.3 mmol) of 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2bromoacetyl) hydrazide (19), prepared as described in Example 19 above, in 75 mL of tetrahydrofuran (THF) was added 1.25 g (7.5 mmol) of triethylphosphite and 0.15 g (1 mmol) of Nal. After 22 hours of refluxing, an additional 0.62 g (3.75 mmol) of triethylphosphite and 0.05 g (0.33 mmol) of NaI were added to the reaction, which was refluxed an additional 24 hours. The solvent was then removed under aspirator vacuum, and the reaction mixture was chromatographed to yield 2.46 g (83%) of 8-chlorodibenz-[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[(diethoxyphosphinyl)acetyl]hydrazide (20), which was a beige foam. Analysis calculated for C20H23N23O6PCl (M.W. 467.85): C, 51.35; H, 4.96; N, 8.98; Cl, 7.58. Found: C, 51.02; H, 5.03; N, 8.83; Cl, 7.39.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05182272 |
|---|
| Source dataset | uspto-grants-1993_01 |
|---|
| ORD ID | ord-18dfae63b19d4ed29008c60c1be364bb |
|---|
| Source note | uspto-grants-1993_01 |
|---|