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HRID 1768791Erstellt: 27. Oktober 2026

8-chlorodibenz[b,f][1,4]oxazepin-10(11H)carbonyl chloride → 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)carboxylic acid

https://huagongshe.com/reaction/1768791

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt8-chlorodibenz[b,f][1,4]oxazepin-10(11H)carbonyl chlorideHCID 14975983—
Edukt8-chlorodibenz[b,f][1,4]oxazepine-10(11H)carboxylic acid, 2-[1-oxo-3-(2-pyridinyl)propyl]hydrazideHCID 14975985—
Eduktalpha,alpha-Difluoro-beta-hydroxy-3-(4-pyridinyl)-propanoic acid, hydrazideHCID 14976002—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelHydrochloric AcidHCID 313—
Produkt8-chlorodibenz[b,f][1,4]oxazepine-10(11H)carboxylic acidHCID 21983467—

Reaktionsschritte

The free base of 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[2,2-difluoro-3-hydroxy-1-oxo-3-(4-1-oxo-3-(4-pyridinyl) propyl]hydrazide (51) was prepared in the same manner as 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[1-oxo-3-(2-pyridinyl)propyl]hydrazide (6), as described above in Example 6, on a 1.75 mmol scale from α,α-difluoro-β-hydroxy-3-(4-pyridinyl)-propanoic acid, hydrazide (50), prepared in the manner described above in Example 50, and 8-chlorodibenz-[b,f][1,4]oxazepine-10 (10H)-carbonyl chloride (2), prepared in the manner described above in Example 2, for a yield of 0.098 g (12%) of product. The free base was taken up in acetic acid (1.5 mL) and 1M HCl (1.5 mL). The material was lyophilized to yield 0.049 mg of the hydrochloride salt. Analysis calculated for C22H17N4O4F2Cl.HCl.0.25 H2O (M.W. 514.83): C, 51.23; H, 3.62; N, 10.86. Found: C, 50.85; H, 3.67; N, 10.94.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05378840
Quelldatensatzuspto-grants-1995_01
ORD IDord-96a7019f5be84f2fbe49903f12a10bc8
Quellennotizuspto-grants-1995_01