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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900584Generated: October 30, 2026

8-chlorodibenz[b,f][1,4]oxazepin-10(11H)carbonyl chloride → HCID 86748368, compound

https://huagongshe.com/reaction/1900584

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-chlorodibenz[b,f][1,4]oxazepin-10(11H)carbonyl chlorideHCID 14975983—
ReactantHCID 14976003HCID 14976003—
ReactantHCID 86748367HCID 86748367—
ProductHCID 86748368HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05576315
Source datasetuspto-grants-1996_11
ORD IDord-075b90ab65ea4ef481e899440cca441d
Source noteuspto-grants-1996_11