With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.78648-27-8,2-(Pyrrolidin-1-yl)benzoic acid,as a common compound, the synthetic route is as follows.,78648-27-8
1- [3- (DIMETHYLAMINO) PROPYL]-3-ETHYLCARBODIIMIDE (0.19 g) was added to a solution of 1- (2-PYRIDINYLACETYL)-5- indolinamine (0.25 g), 2- (1-PYRROLIDINYL) benzoic acid (0.23 g), 1-hydroxybenzotriazole hydrate (0.16 g) and 4- dimethylaminopyridine (6 mg) in N, N-dimethylformamide (5 ml) under ice-cooling and the mixture was stirred at ambient temperature for 18 hours. The reaction mixture was poured into a mixture of ethyl acetate and water. The separated organic layer was washed with water, dried over magnesium sulfate and evaporated in vacuo. The residue was triturated with ethyl acetate to give N- [1- (2-PYRIDINYLACETYL)-2, 3- DIHYDRO-LH-INDOL-5-YL]-2- (L-PYRROLIDINYL) benzamide (0.27 g). 1H-NMR (DMSO-d6): 8 1. 75-1. 95 (4H, m), 3.08-3. 29 (4H, m), 3.16 (2H, t, J=8.4 Hz), 4.00 (2H, s), 4.21 (2H, t, J=8.4 Hz), 6.65-6. 82 (2H, m), 7.21-7. 47 (5H, m), 7.69 (1H, s), 7.76 (1H, dt, J=1.8 Hz, 7.6 Hz), 7.96 (1H, d, J=8.7 Hz), 8.50 (1H, dd, J=0.9 Hz, 4.2 Hz), 10.27 (1H, s) (-) ESI-MS: 425 (M-H)-
The synthetic route of 78648-27-8 has been constantly updated, and we look forward to future research findings.
Reference£º
Patent; FUJISAWA PHARMACEUTICAL CO., LTD.; DAISO CO., LTD.; WO2004/39795; (2004); A2;,
Pyrrolidine – Wikipedia
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