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Chemical Structure| 138112-76-2 Chemical Structure| 138112-76-2
Chemical Structure| 138112-76-2

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Agomelatine is a melatonin structurely similar 5-HT2C receptor antagonist as well as a potent melatonin receptor agonist, used to treat major depressive disorder.

Synonyms: S-20098

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Product Details of Agomelatine

CAS No. :138112-76-2
Formula : C15H17NO2
M.W : 243.30
SMILES Code : CC(NCCC1=C2C=C(OC)C=CC2=CC=C1)=O
Synonyms :
S-20098
MDL No. :MFCD00916659
InChI Key :YJYPHIXNFHFHND-UHFFFAOYSA-N
Pubchem ID :82148

Safety of Agomelatine

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of Agomelatine

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 138112-76-2 ]

[ 138112-76-2 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 108-24-7 ]
  • [ 138113-08-3 ]
  • [ 138112-76-2 ]
YieldReaction ConditionsOperation in experiment
89% With hydrogen;Raney nickel; In ethanol; water; at 70℃; under 22502.3 Torr; Step C: N-[2-(7-Methoxy-1-naphthyl)ethyl]acetamide There are introduced into an 8 litre reactor 136 g of Raney nickel, 2.06 litres of ethanol and 0.23 litre of water. Whilst stirring at 70 C. and under 30 bars of hydrogen, the compound obtained in Step B (0.8 kg), dissolved in acetic anhydride (2.4 litres), is added slowly. At the end of the addition, the reaction mixture is stirred for 1 hour under hydrogen at 30 bars; the reactor is then subjected to decompression and the liquors are filtered. After concentrating the mixture, the residue is crystallized from an ethanol/water 35/65 mixture to yield the title product in a yield of 89% and with a chemical purity of more than 99%. Melting point: 108 C.
89% With hydrogen; In ethanol; water; at 70℃; under 22502.3 Torr; The reaction was carried out on a larger batch in order to optimise the yield obtained: 136 g of Raney nickel, 2.06 L of ethanol and 0.23 L of water are introduced into an 8 L reactor. Whilst stirring at 70 C. and under 30 bars of hydrogen, the compound obtained in Step D (0.8 kg) dissolved in acetic anhydride (2.4 L) is slowly added. At the end of the addition, the reaction mixture is stirred for 1 hour under hydrogen at 30 bar, the reactor is then decompressed and the liquors are filtered. After concentration of the mixture, the residue is crystallised from a mixture of ethanol/water 35/65 to yield the title product in a yield of 89% and with a chemical purity greater than 99%. Melting point: 108 C.
89% With hydrogen; In ethanol; water; at 70℃; under 22502.3 Torr; for 1h; 136 g of Raney nickel, 2.06 L of ethanol and 0.23 L of water are introduced into an 8-L reactot Whilst stirring at 70 C. and under 30 bars of hydrogen, the compound obtained in Step D above (0.8 kg) dissolved in acetic anhydride (2.4 L) is added slowly. When the addition is complete, the reaction mixture is stirred for 1 hour under hydrogen at 30 bars, and then the reactor is depressurised and the liquors are filtered. Afier concentration of the mixture, the residue is crystallised from a mixture of ethanol/water 35/65 to yield the title product in a yield of 89% and with a chemical purity greater than 99%.10075] Melting point: 108 C. ?H NMR spectroscopic analysis (CD3OD, 300.13MHz, oe in ppm): 8.21 (bs, 1H); 7.74 (d, J=8.9 Hz, 1H); 7.65 (d, J=8.0 Hz, 1H); 7.52 (d, J=2.5 Hz, 1H); 7.31-7.2 (m, 2H); 7.11 (dd, J=8.9 and 2.5 Hz, 1H); 3.96 (s, 3H); 3.52-3.44 (m, 2H); 3.23-3.18 (m, 2H); 1.94 (s, 3H). ?3C NMR spectroscopic analysis (CD3OD, 75.5 MHz, oe in ppm): 173.4 (s); 159.4 (s); 135.1 (s); 134.6 (s); 131.2 (d); 130.8 (s); 128.2 (d); 127.9 (d); 124.2 (d); 119.3 (d); 103.2 (d); 55.9 (q); 41.4 (0; 34.2 (0; 22.6 (q).
In 10L reactor 2-(7-methoxynaphthalen-1 -yl)acetonitrile (750g), methanol (6,3L), NaOH solution (228g NaOH is diluted in 750ml_ water) and 134g of Raney-Nickel is charged. Reaction mixture is stired at 30C and 4 bar H2 and monitored with HPLC. After reaction is done, it is cooled to 15C and acetic anhydride (750mL) is added and warmed to 25C. Reaction is monitored with HPLC. Once the reaction is finished it is filtered, solvent evaporated, than ethyl acetate (5L) is added and organic phase is extracted with water (5L). Solvent is evaporated to obtain agomelatine of 96,4% HPLC purity.

 

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