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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 585750Erstellt: 25. Oktober 2026

4-Aminopyridine → 4-(tert-butoxycarbonylamino)-6-methyl-N-(4-pyridyl)thiochromane-7-carboxamide

https://huagongshe.com/reaction/585750

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-AminopyridineHCID 1727—
Edukt2-Chloro-1-methylpyridinium iodideHCID 167069—
Edukt4-(Tert-butoxycarbonylamino)-6-methylthiochromane-7-carboxylic acidHCID 22337379—
Produkt4-(tert-butoxycarbonylamino)-6-methyl-N-(4-pyridyl)thiochromane-7-carboxamideHCID 2233737767,5%

Reaktionsschritte

By a similar reaction operation as in Starting Material Synthetic Example 53 using 4-(tert-butoxycarbonylamino)-6-methylthiochromane-7-carboxylic acid (1.00 g), 4-aminopyridine (321 mg) and 2-chloro-1-methylpyridinium iodide (949 mg), the objective 4-(tert-butoxycarbonylamino)-6-methyl-N-(4-pyridyl)thiochromane-7-carboxamide (834 mg) was obtained as colorless crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06933305B2
Quelldatensatzuspto-grants-2005_08
ORD IDord-377a95a185fe48a086ff3b6818dac67d
Quellennotizuspto-grants-2005_08