JNJ-42847922 synthesis - chemicalbook

1186050-58-7 Synthesis

2-Fluoro-6-(2H-1,2,3-triazol-2-yl)benzoic acid

1186050-58-7
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Pyrrolo[3,4-c]pyrrole, 2-(4,6-dimethyl-2-pyrimidinyl)octahydro-

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-

Yield: 74%

Reaction Conditions:

with thionyl chloride;sodium carbonate;sodium hydroxide in water;toluene at 0 - 50; for 4.5 h;Inert atmosphere;

Steps:

107.A
To a 3-necked, 3 L, round- bottomed flask equipped with a nitrogen line, temperature probe, heating mantle, reflux condenser, mechanical stirrer, and 1 N aq. NaOH scrubber were added 2-fluoro-6-[1 ,2,3]triazol-2-yl-benzoic acid (Intermediate 12, 120.98 g, 75 wt%, 90.74 g actual, 438 mmol) and toluene (1 L). The mixture was warmed to 50 ^oC for 1 h with stirring. The mixture was then cooled to 25 ^oC and thionyl chloride (47.9 mL, 657 mmol) was added. The mixture was warmed back to 50 ^oC and held for 1 h. During this time, in a separate 5 L jacketed reactor equipped with a mechanical stirrer and temperature probe were added toluene (600 mL), aqueous sodium carbonate (185.7 g, 1 .75 mol in 1 .6 L water), and 2- (4,6-dimethyl-pyrimidin-2-yl)-octahydro-pyrrolo[3,4-c]pyrrole*HOAc(Intermediate 23, 122 g, 438 mmol). This biphasic mixture was cooled to 0 ^oC. After cooling to 0 ^oC, the original slurry was poured through a filter and over the stirring biphasic mixture of amine and aqueous sodium carbonate. The mixture was allowed to warm to room temperature. After 2 h, additional 2-(4,6- dimethyl-pyrimidin-2-yl)-octahydro-pyrrolo[3,4-c]pyrrole*HOAc (4 g, 14 mmol) was added and the mixture was stirred for 30 additional minutes. At the end of this period, the layers were separated and 100 mL of methanol were added to the organic layer. The organic layer was dried over MgSO , filtered, and concentrated to a white solid. This solid was taken up in ethanol (1 .4 L) and warmed to 77 ^oC. The mixture was then cooled to 55 ^oC and seeded with previously crystallized material. (Note: The seeds were generated from slurrying the initial product in 2-propanol at room temperature [100 mg/mL]). The mixture was cooled to room temperature at a rate of 5 ^oC per hour. After stirring at room temperature for 14 h, the mixture was filtered and dried to provide the final product as a white crystalline solid (136.84 g, 74%). ¹H NMR (400 MHz, CDCIs): 7.88 - 7.78 (m, 1 .78H), 7.75 - 7.69 (s, 1 .22H), 7.51 - 7.43 (m, 1 H), 7.17 - 7.1 1 (m, 1 H), 6.30 - 6.28 (m, 1 H), 4.03 - 3.48 (m, 7H), 3.29 - 3.21 (m, 1 H), 3.15 - 2.92 (m, 2H), 2.30 (s, 6H). MS (ESI) mass calcd forC21 H22FN₇O, 407.19; m/z found, 408 [M+H]⁺. Anal, calcd. for C21 H22FN₇O C, 61 .90, H, 5.44, N, 24.06; found C, 61 .83, H, 5.42, N, 24.08

References:

Location in patent:Page/Page column 144-145

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5-Benzyl-2-Boc-hexahydro-pyrrolo[3,4-C]pyrrole

186202-73-3
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References

141449-85-6
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References

Ethanamine, N-[(3,5-dichlorophenyl)methylene]-2,2-diethoxy-

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References