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4-(4-oxo-3,4-dihydroquinazolin-2-yl)butanoic acid(SALTDATA: FREE) synthesis

8synthesis methods
-

Yield:95494-51-2 88.3%

Reaction Conditions:

in toluene; for 3 h;Reflux;

Steps:

1.1 Example 1: Pilot synthesis process of SPAM1 (two-step method)

As shown in Figure 1, a two-step synthesis is used. Step 1: In a 150 mL flask equipped with a condenser, benzamide A (5.45 g, 40.0 mmol, 1.0, etc.) and amber hydride B (4.00 g, 40.0 mmol, 1.0, etc.) are mixed with 50 mL of toluene in. The suspension was refluxed vigorously for 3 hours and then cooled to room temperature. The resulting product C was a white solid which was filtered, washed with Et2O and dried (8.833 g, yield 88.3%). The product NMR detection is shown in Figure 2.

References:

CN111533702,2020,A Location in patent:Paragraph 0037-0038