Reaktion #66732

Reaktionsgleichung

sodium hydride

1-benzyloxy-7-chloro-6-fluoro-isoquinoline

1-Benzyloxy-7-chloro-6-fluoro-isoquinoline

4-amino-adamantan-1-ol

→

title compound

Ausbeute 31.2%

5-(1-Benzyloxy-7-chloro-isoquinolin-6-yloxy)-adamantan-2-ylamine

Ausbeute 31.2%

Lösungsmittel

dimethyl acetamide

dimethyl acetamide

dimethyl acetamide

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGstirring
2. 2
   Sonstigewas continued at room temperature until the reaction
3. 3
   SonstigeThe reaction was quenched by addition of water (15 mL)
4. 4
   Extraktionthe reaction mixture was extracted twice with a mixture of dichloromethane and 2-propanol (3:1)
5. 5
   SonstigeThe combined organic layers were evaporated
6. 6
   workup.ADDITIONwater was added
7. 7
   Sonstigeto remove remainders of dimethyl acetamide
8. 8
   SonstigeThe obtained crude product
9. 9
   Sonstigewas purified by flash chromatography (SiO2, 0%→30% methanol in dichloromethane)

Vorschrift

To a suspension of sodium hydride (60% in mineral oil, 417 mg, 10.4 mmol, 3 eq.) in dimethyl acetamide (7 mL) was added a solution of 4-amino-adamantan-1-ol (640 mg, 3.82 mmol, 1.1 eq.) in dimethyl acetamide (7 mL). After stirring for 60 min at room temperature, a solution of 1-benzyloxy-7-chloro-6-fluoro-isoquinoline (1, 1.0 g, 3.48 mmol) in dimethyl acetamide (7 mL) was added and stirring was continued at room temperature until the reaction went to completion. The reaction was quenched by addition of water (15 mL) and the reaction mixture was extracted twice with a mixture of dichloromethane and 2-propanol (3:1). The combined organic layers were evaporated, water was added and the mixture was subjected to lyophilization to remove remainders of dimethyl acetamide. The obtained crude product was purified by flash chromatography (SiO2, 0%→30% methanol in dichloromethane) to yield 473 mg of the title compound as diastereomeric mixture. Rt=1.35 min, 1.55 min (Method 3). Detected mass: 435.2 (M+H+).

Quelle