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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 419896Erstellt: 26. Oktober 2026

2-Nitrobenzoyl chloride → 2-(2-Nitrophenyl)thiazolo[4,5-c]pyridine

https://huagongshe.com/reaction/419896

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Nitrobenzoyl chlorideHCID 11875—
EduktPhosphorus sulfide (P2S5)HCID 14817—
Edukt3-Amino-4-hydroxypyridineHCID 233392—
EduktHCID 178513633HCID 178513633—
LösungsmittelPyridineHCID 1049—
LösungsmittelP-XyleneHCID 7809—
Produkt2-(2-Nitrophenyl)thiazolo[4,5-c]pyridineHCID 5968018855%
ProduktHCID 178522382HCID 178522382—

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

N-(4-Hydroxy-pyridin-3-yl)-2-nitro-benzamide was prepared using a procedure similar to that described above using 4-hydroxy-3-aminopyridine and 2-nitrobenzoyl chloride. A mixture of -(4-Hydroxy-pyridin-3-yl)-2-nitro-benzamide (2.6 g, 0.01 mol) and P2S5 (4.44 g, 0.02 mol) in pyridine (12.5 mL) and p-xylene (50 mL) was stirred at 140° C. for 18 hrs. The solvent was removed under vacuo and the residue was purified by recrystallization to give 2-(2-nitrophenyl)thiazolo[4,5-c]pyridine as a yellow solid (1.43 g, yield: 55%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093401B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-c23f9f805b164c438f523845523d1c2a
Quellennotizuspto-grants-2012_01