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HRID 2080992Erstellt: 25. Oktober 2026

p-Toluenesulfonic acid monohydrate → HCID 178433271, Verbindung

https://huagongshe.com/reaction/2080992

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Toluenesulfonic acid monohydrateHCID 521998—
EduktN-[(2-Chloro-3,4-difluorophenyl)methyl]-3-methyl-2-oxo-4-imidazolidinecarboxamideHCID 25098282—
EduktHCID 178433279HCID 178433279—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktHCID 178433271HCID 17843327174%

Reaktionsschritte

A solution of N-[(2-chloro-3,4-difluorophenyl)methyl]-3-methyl-2-oxo-4-imidazolidinecarboxamide (152 mg, 0.5 mmol) (prepared as described in Example 28), (4-methyl-1H-imidazol-5-yl)methanol hydrochloride (93 mg, 0.625 mmol) and p-toluene sulfonic acid monohydrate (19 mg, 0.100 mmol) in N-methyl-2-pyrrolidone (1 ml) was heated at 130° C. under argon for 3 h. The reaction mixture was cooled to room temperature and diluted with dichloromethane. The solution was washed with saturated sodium hydrogen carbonate solution and brine, dried and evaporated. The residue was purified by mass-directed automated HPLC, followed by trituration with ether to give N-[(2-chloro-3,4-difluorophenyl)methyl]-3-methyl-1-[(4-methyl-1H-imidazol-5-yl)methyl]-2-oxo-4-imidazolidinecarboxamide (147 mg, 74%). LC/MS [M+H]+=398, retention time=1.57 minutes.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07932282B2
Quelldatensatzuspto-grants-2011_04
ORD IDord-07145fe5a9d647ceb0743b1767052f77
Quellennotizuspto-grants-2011_04