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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1184654Erstellt: 27. Oktober 2026

2-Chloroethyl isocyanate → {7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl} (2-chloroethyl)carbamate

https://huagongshe.com/reaction/1184654

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Chloroethyl isocyanateHCID 16035—
EduktTolvaptanHCID 216237—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelTolueneHCID 1140—
Produkt{7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl} (2-chloroethyl)carbamateHCID 8670893782%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Tolvaptan (1.0 g, 2.2 mmol) was suspended in toluene (7 ml). 2-Chloroethyl isocyanate (0.28 ml, 3.3 mmol) and 4-dimethylaminopyridine (DMAP) (27 mg, 0.22 mmol) were added thereto, and the mixture was stirred at 80° C. for 24 hours. After cooling to room temperature, the insoluble materials were filtered off and washed with ethyl acetate. The filtrate was concentrated under reduced pressure. The residue was purified by silica gel flash chromatography (n-hexane:ethyl acetate=54:46→33:67). The purified product was concentrated under reduced pressure to obtain 1.0 g of {7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl}(2-chloroethyl)carbamate as white amorphous solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08669229B2
Quelldatensatzuspto-grants-2014_03
ORD IDord-9557162d57b747b49db1b568ee972bde
Quellennotizuspto-grants-2014_03