Analyzing the synthesis route of N-(5-Bromopentyl)phthalimide

The synthetic route of 954-81-4 has been constantly updated, and we look forward to future research findings.

Reference of 954-81-4, These common heterocyclic compound, 954-81-4, name is N-(5-Bromopentyl)phthalimide, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

To a stirred solution of compound 14-k (80 g, 0.27 mol) in DMF (745 mL) was added potassium thioacetate (34 g, 0.29 mol) portion wise over 20 mm at room temperature .Afier complete addition, the reaction mixture was stirred at room temperature for 30 mm. Reaction progress was monitored by TLC; after completion the reaction mixture was quenched with ice-cold water (1 L) and stirred for I h. The resultant precipitate was filtered, washed with water (500 rnL) and dried in vacuo to afford 15-k as an off-white solid (75 g, 95%).?H NMR (40() MHz, C1)Ci3): d 7.84 (dd, J= 5.5 Hz, 3.() Hz, 2K), 7.71 (dd, j:zr. 5.5 Hz, 3.1 Hz, 2H), 3.67 (t, J= 7.3 Hz, 2H), 2.85 (t, J= 7.3 Hz, 2H), 2.30 (s, 3H), 1.73-1.65 (m, 3H), 1.64-1.57 (m, 1Ff), 1.46-1.37 (m, 2H);LC-MS: 292.2 (M+1).

The synthetic route of 954-81-4 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; CV6 THERAPEUTICS (NI) LIMITED; SPYVEE, Mark; SHIRUDE, Pravin S.; (258 pag.)WO2017/6282; (2017); A1;,
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