Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 336981Erstellt: 25. Oktober 2026

Methanol → 2-Amino-7-hydroxyisoquinolinium 2,4,6-trimethylbenzenesulfonate

https://huagongshe.com/reaction/336981

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Edukt7-IsoquinolinolHCID 459767—
Edukt2-Aminoisoquinolinium IodideHCID 10858601—
EduktO-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamineHCID 11830845—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Amino-7-hydroxyisoquinolinium 2,4,6-trimethylbenzenesulfonateHCID 11769929860,5%

Reaktionsschritte

O-mesitylene sulfonyl hydroxylamine (MSH) (3) was used to prepare the N-amino salt as an aminating agent as described by Tamura et al., (1972) Tetrahedron Letter. 40: 4133, incorporated herein by reference in its entirety. An ice cooled solution of 7-hydroxyisoquinoline (2.0 g, 13.78 mmol) in 30 mL of dry methylene chloride, and 15 ml of dry methanol was added drop wise to O-mesitylenesulfonylhydroxylamine (2.97 g, 13.78 mmol) in 10 mL of dry methylene chloride over 5 min with stirring. The reaction stirred at 0° C. for 6 h. 70 mL of ether was added and the suspension filtered. The precipitate was recrystallized from ethyl acetate to give 2-amino-7-hydroxyisoquinolinium 2,4,6-trimethylbenzenesulfonate (6) in 60.5% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889713B1
Quelldatensatzuspto-grants-2014_11
ORD IDord-dc6594f54f0146059ab7c1b506b027da
Quellennotizuspto-grants-2014_11