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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1938552Erstellt: 24. Oktober 2026

Methanesulfonic Acid → 2-(4-Carboxypiperidino)-4-(3,4-methylenedioxy-benzyl)amino-6-chloroquinazoline methanesulfonate

https://huagongshe.com/de/reaction/1938552

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanesulfonic AcidHCID 6395—
Edukt1-(6-Chloro-4-(3,4-methylenedioxybenzyl)aminoquinazolin-2-yl)piperidine-4-carboxylic acidHCID 5311486—
LösungsmittelEthanolHCID 702—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(4-Carboxypiperidino)-4-(3,4-methylenedioxy-benzyl)amino-6-chloroquinazoline methanesulfonateHCID 2118403290,7%

Reaktionsschritte

2.00 g (4.54 mmol) of the 2-(4-carboxypiperidino)-4-(3,4-methylenedioxybenzylamino)-6-chloroquinazoline prepared in Example 222 was dissolved in a mixture comprising 25 ml of tetrahydrofuran and 25 ml of ethanol under heating, followed by the dropwise addition of 0.31 ml (4.78 mmol) of methanesulfonic acid. The obtained mixture was cooled by allowing to stand to precipitate crystals. The crystals were recovered by filtration, washed with tetrahydrofuran, and air-dried to give 2.21 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05693652
Quelldatensatzuspto-grants-1997_12
ORD IDord-b81665562bfd469bb00e23b65d005a11
Quellennotizuspto-grants-1997_12