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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2277655Erstellt: 25. Oktober 2026

Ammonia → 4-Bromo-5,6,7,8-tetrahydroisoquinolin-8-amine

https://huagongshe.com/reaction/2277655

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktMethanolHCID 887—
EduktSodium borohydrideHCID 4311764—
Edukt4-Bromo-6,7-dihydro-8(5H)-isoquinolinoneHCID 71743380—
KatalysatorTitanium isopropoxideHCID 11026—
Produkt4-Bromo-5,6,7,8-tetrahydroisoquinolin-8-amineHCID 7174337985%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

4-Bromo-6,7-dihydroisoquinolin-8(5H)-one (intermediate B-11 [C]) (4.81 g, 21.3 mmol), titanium (IV) isopropoxide (12.1 g, 42.6 mmol) and ammonia, 2.0 M solution in MeOH (53.2 mL, 106 mmol) were stirred at room temperature for 5 h. The reaction was cooled to 0° C. and NaBH4 (1.21 g, 31.9 mmol) was added portionwise over 10 min; the resulting mixture was stirred at room temperature for an additional 2 h. The reaction was quenched by pouring it into aq ammonium hydroxide 25%, the precipitate was filtered and washed with EtOAc (3×, each time suspended in AcOEt and stirred for 5 min). The organic layer was separated and the remaining aqueous layer was extracted with EtOAc. The combined organic extracts were extracted with 1 M HCl. The acidic aqueous extracts were washed with ethyl acetate (1×), then treated with aqueous sodium hydroxide (2 M) to give pH 10-12 and extracted with EtOAc (3×). The combined organic extracts were washed with brine, dried (Na2SO4), and concentrated in vacuo to afford the title compound (4.11 g, 85%) as brown solid. MS: 225 (M+, 1Br).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09133158B2
Quelldatensatzuspto-grants-2015_09
ORD IDord-43ba7f842f0f4b03953bd109086abdd0
Quellennotizuspto-grants-2015_09