Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 128653Erstellt: 23. Oktober 2026

8-chlorodibenz[b,f][1,4]oxazepin-10(11H)carbonyl chloride → SC-51322

https://huagongshe.com/de/reaction/128653

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—
Edukt3-[(2-Furanylmethyl)thio]propanoic acid, hydrazideHCID 63580095—
ProduktSC-51322HCID 9933831—

Reaktionsschritte

8-chlorodibenz[b,f][1,41oxazepine-10(11H)-carboxylic acid, 2-[3-[(2-furanylmethyl)thio]-1-oxopropyl]hydrazide (13) was prepared in the manner 8-chlorodibenz[b,f]oxazepine-10(11H)-carboxylic acid, 2-[1-oxo-3-(2-pyridinyl)propyl]hydrazide (6) was prepared, as described above in Example 6, from 3-[(2-furanylmethyl)thio]propanoic acid, hydrazide (12), prepared as described above in Example 12, and 8-chlorodibenz[b,f][1,4]-oxazepine-10(11H)-carbonyl chloride (2), prepared as described above in Example 2, on a 10 mmol scale. The yield was quantitative. Analysis calculated for C22H20N3O4SCl (M.W. 457.94): C, 57.70; H, 4.40; N, 9.18; Cl, 7.74; S, 7.00. Found: C, 57.59; H, 4.36; N, 9.01; Cl, 7.95; S, 7.07.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05464830
Quelldatensatzuspto-grants-1995_11
ORD IDord-49200922f7c94b7b8d05ad8d2df8cf6e
Quellennotizuspto-grants-1995_11