Methanol → HCID 86661589, compound

To a solution of methyl 3-fluoro-5-iodo-4-methylbenzoate (115.5 g, 392.8 mmol) in toluene (˜1600 mL) at ambient temperature was charged benzophenone imine (67.6 g, 373.0 mmol), 1,1′-bis(diphenylphosphino)ferrocene (9.80 g, 17.68 mmol) and cesium carbonate (179.2 g, 550.0 mmol). The reaction vessel was vacuum purged with nitrogen three times. Tris(dibenzylideneacetone)dipalladium(0) (5.34 g, 6.05 mmol) was added before the vessel was again vacuum purged with nitrogen three times. The reaction mixture was then stirred and heated to reflux for 4 d before being cooled to ambient temperature and filtered through GF/F filter paper under a nitrogen atmosphere. The filter cake was washed with toluene (230 mL) and the filtrates combined and washed with aq. sodium sulfite (5% w/w, 580 mL). The phases were separated and the aq. phase re-extracted with toluene (580 mL). The organic fractions were combined and washed with water (580 mL), dried over sodium sulfate and filtered through GF/F filter paper. The filter cake was washed with toluene (230 mL) and the combined filtrates concentrated to ˜1000 mL in vacuo. After cooling the solution to ambient temperature, TBME (1040 mL) was charged followed by decolourising charcoal (60 g). The slurry was heated to 45-50° C. and then cooled to ambient temperature over 1 h and filtered through GF/F filter paper. The filter cake was washed with TBME/toluene (1:1 v/v, 2×230 mL). The filtrates were combined to afford a solution of methyl 3-[(diphenylmethylene)amino]-5-fluoro-4-methylbenzoate to which methanol (127 mL, 3135.4 mmol) was added. Sulfuric acid (21 mL, 394.0 mmol) was then charged over at least 1 h ensuring that the temperature was maintained in the range 18-23° C. The resulting slurry was filtered through 100 μm cloth. The filter cake was washed with TBME (580 mL) and dried on the filter under a flow of nitrogen for at least 2 h. The isolated solid was then slurried in acetonitrile (500 mL) at ambient temperature for 4-5 h before being filtered through 100 μm cloth. The filter cake was washed with acetonitrile (1×300 mL, 1×115 mL) and dried on the filter at up to 45° C. to afford methyl 3-amino-5-fluoro-4-methylbenzoate sulfuric acid salt (92.2 g, 94.5% w/w).

1. custompurged with nitrogen three times
2. custompurged with nitrogen three times
3. temperatureheated
4. temperatureto reflux for 4 d
5. filtrationfiltered through GF/F
6. filtrationfilter paper under a nitrogen atmosphere
7. washThe filter cake was washed with toluene (230 mL)
8. washwashed with aq. sodium sulfite (5% w/w, 580 mL)
9. customThe phases were separated
10. extractionthe aq. phase re-extracted with toluene (580 mL)
11. washwashed with water (580 mL)
12. dry with materialdried over sodium sulfate
13. filtrationfiltered through GF/F
14. filtrationfilter paper
15. washThe filter cake was washed with toluene (230 mL)
16. concentrationthe combined filtrates concentrated to ˜1000 mL in vacuo
17. temperatureAfter cooling the solution to ambient temperature
18. additionTBME (1040 mL) was charged
19. temperatureThe slurry was heated to 45-50° C.
20. temperaturecooled to ambient temperature over 1 h
21. filtrationfiltered through GF/F
22. filtrationfilter paper
23. washThe filter cake was washed with TBME/toluene (1:1 v/v, 2×230 mL)

ORD record

ord-8d450303d5274304ba5495585854eb5b

Source dataset

uspto-grants-2015_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08969350B2