ChemicalBook CAS DataBase List MLN-8237

MLN-8237 synthesis

6synthesis methods

Product Name:MLN-8237
CAS Number:1028486-01-2
Molecular formula:C27H20ClFN4O4
Molecular Weight:518.92

4-Guanidino-2-methoxybenzoic Acid Hydrochloride

1028486-08-9
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(1E,4E)-8-chloro-4-((diMethylaMino)Methylene)-1-(2-fluoro-6-Methoxyphenyl)-3,4-dihydrobenzo[c]azepin-5-one

869367-33-9
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1028486-01-2
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Yield:1028486-01-2 80%

Reaction Conditions:

Stage #1:4-{[amino(imino)methyl]amino}-2-methoxybenzoic acid hydrochloride;8-chloro-4-[(dimethylamino)methylene]-1-(2-fluoro-6-methoxyphenyl)-3,4-dihydro-5H-2-benzazepin-5-one with potassium carbonate in methanol at 50 - 55; for 24 h;
Stage #2: with hydrogenchloride in methanol;water; pH=3 at 20 - 55; for 2 h;

Steps:

3.4
4-{f9-chloro-7-(2-fluoro-6-methoxyphenyl)-5H-pyrimido[5,4-rf1[2lbenzazepin-2- ynamino)-2-methoxybenzoic acid (Formula II)[0156] Into a reactor was added 6 (3.81kg, 15.5mol), potassium carbonate (4.3kg, 31.1mol), 9 (5.27kg, 14.1mol) and methanol (63L). The suspension was warmed to 50 to 55 °C and stirred for a minimum of 24h until >96.0% conversion was obtained by HPLC analysis. Methanol (10L) and water (37L) were added while maintaining the temperature between 50 and 55 °C. The pH of the mixture was adjusted to 3.0 to 4.0 using 7% w/ w HC1 (prepared from 7.0kg of concentrated HQ and 24L of water) while maintaining the temperature between 50 and 55 °C. The suspension was cooled to 20 to 25 °C over a minimum of lh and stirred for at least 60min. The resulting suspension was filtered and washed with water (2 x 26.3L) at 50 to 55 °C and methanol (2 x 10L) at 20 to 25 °C. The wet cake was dried at 45 to 50 °C under vacuum to provide 5.85kg (80% yield) of Formula (II). ? NMR (300 MHz, DMSO-d₆) δ 12.07 (s, IH), 10.22(s, IH), 8.72 (s, IH), 8.29 (d, J=8.8 Hz, IH), 7.95 (s, IH), 7.80 (dd, J=2.4, 8.9 Hz, IH), 7.70 (d, J=8.8 Hz, IH), 7.39 (m, 3H), 7.21 (s, IH), 6.89 (s, 2H), 3.82 (s, 6H); MS (ESI) m/z MS (ESI) m/z 517.2 (M - H⁺, 45%).

References:

MILLENNIUM PHARMACEUTICALS, INC.;ARMITAGE, Ian;COOPER, Martin, I.;EDDLESTON, Mark, D.;FAIBER, Neil, C.;MCCUBBIN, Quentin, J.;WATT, Stephen, W. WO2011/103089, 2011, A1 Location in patent:Page/Page column 45

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869365-97-9 Synthesis