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HRID 2414825Erstellt: 26. Oktober 2026

1-(4-Fluoro-benzyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline → HCID 69763736, Verbindung

https://huagongshe.com/reaction/2414825

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(4-Fluoro-benzyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinolineHCID 37411—
EduktDiisopropylethylamineHCID 81531—
Edukttert-Butyl N-(2-bromoethyl)carbamateHCID 4103526—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 69763736HCID 69763736—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

To a solution of 1-(4-fluorobenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline (example A31, 1.05 g, 3.5 mmol) in THF (40 mL) is added (2-bromo-ethyl)-carbamic acid tert-butyl ester (example B1, 0.94 g, 4.2 mmol) and DIPEA. The reaction mixture is stirred at 70° C. in a sealed flask for 5 days. After cooling to rt, the reaction mixture is evaporated to dryness, and the residue is purified by preparative HPLC to provide the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06815451B2
Quelldatensatzuspto-grants-2004_11
ORD IDord-cf33ce8e019049ccb201b8713b078e9f
Quellennotizuspto-grants-2004_11