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ChemicalBook CAS DataBase List (S)-2-(1-aMinopropyl)-5-fluoro-3-phenylquinazolin-4(3H)-one

(S)-2-(1-aMinopropyl)-5-fluoro-3-phenylquinazolin-4(3H)-one synthesis

7synthesis methods
870281-85-9 Synthesis
(S)-tert-butyl (1-(5-fluoro-4-oxo-3-phenyl-3,4-dihydroquinazolin-2-yl)propyl)carbaMate

870281-85-9
96 suppliers
$29.00/1g

-

Yield:870281-86-0 100%

Reaction Conditions:

with hydrogenchloride in water;ethyl acetate at 20;

Steps:

39.4 Step 4) (S) -2- (1-Aminopropyl) -5-fluoro-3-phenylquinazolin-4 (3H) -one

The compound (S) - (1- (5-fluoro-4-oxo-3-phenyl-3,4-dihydroquinazolin-2-yl) propyl) carbamic acidTert-butyl ester (220 mg, 0.55 mmol) was dissolved in EtOAc (2 mL) and then a solution of hydrogen chloride in ethyl acetate (2.5 mL, 3.88 M) was added in one portion at room temperature. The resulting mixture was stirred at rt overnight, the resulting suspension was dissolved in water (20 mL) and the aqueous phase was extracted with EtOAc (20 mL) and Na2CO3 powder adjusted to pH = 8 and extracted with EtOAc (20 mL x 3 ). The combined organic phases were washed with brine (20 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the title compound as a white powder (163 mg, 100%).

References:

CN104513235,2017,B Location in patent:Paragraph 1158; 1159; 1160; 1161

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