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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1072000Erstellt: 26. Oktober 2026

Pyridine → HCID 178440950, Verbindung

https://huagongshe.com/reaction/1072000

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktDimethylformamideHCID 6228—
Edukt4-tert-Butylbenzyl alcoholHCID 13416—
EduktDiisopropylethylamineHCID 81531—
Edukt4-Nitrophenyl chloroformateHCID 82129—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 178440950HCID 178440950—

Reaktionsschritte

To a solution of 4-tert-butylbenzyl alcohol (1.97 g, 12 mmol) in DCM (30 mL) was added pyridine (1.3 mL) and then a solution of 4-nitrophenyl chloroformate (1.57 g, 7.8 mmol) in DCM (20 mL). The mixture was stirred at room temperature for 1 h, concentrated under reduced pressure, and to the residue was added a mixture of of 4,5,6,7-tetrahydromidazo[4,5-c]pyridine (1.5 g, 7 mmol), methanol (3.3 mL), DMF (30 mL), and diisopropylethylamine (4.1 mL). The resulting mixture was stirred at room temperature overnight and concentrated under reduced pressure. The residue was distributed between water and ethyl acetate, phases were separated, and the organic layer was washed with water, dried (MgSO4), and filtered. A solution of oxalic acid (0.63 g) in ethyl acetate was added to the filtrate and the mixture was allowed to stand for 24 h. Filtration yielded the title compound as colorless solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06908926B1
Quelldatensatzuspto-grants-2005_06
ORD IDord-597b2f8d88f84ce8a7442fc7e07d1de4
Quellennotizuspto-grants-2005_06