Hydrochloric Acid → HCID 58757109、化合物

温度

24 °C

Heat a mixture of 6-hydroxy-3-(2,2,2-trifluoroacetyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine (120 g, 0.4629 mol) and toluene (14.4 L) to 70° C. for 45 min until most of the starting material is dissolved. Add diisobutylamine (1.197 g, 1.62 mL, 9.26 mmol) followed by addition of sulfuryl chloride (62.48 g, 37.19 mL, 0.463 mol) in toluene (360 mL) over 20 min. Stir the reaction mixture for 50 min and then add additional sulfuryl chloride (4.536 g, 2.70 mL, 0.0336 mol) neat and stir the reaction mixture for 15 min at 70° C. Cool the reaction mixture to 24° C. over 30 min and then add 1 N HCl (2.00 L). Separate, wash the organic layer with saturated aqueous sodium bicarbonate solution (2.00 L), brine (2.00 L), dry (sodium sulfate) and concentrate using a rotary evaporator at 70° C. until about 672.5 g remains using the minimum effective vacuum in order to maintain a vapor phase sufficient to prevent drying above the solvent line and self-seeding, thus preventing crystallization under these conditions. Using toluene heated to 70° C., transfer the light-yellow solution to a preheated (70° C.) 3-neck flask equipped with a mechanical stirrer. Lower the temperature to 58° C. over 1 h. If available, seed the solution with crystals of 7-chloro-6-hydroxy-3-(2,2,2-trifluoroacetyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine from a prior synthesis to enhance crystallization. After 30 min, reduce the temperature further to 55° C. and observe the initiation of the crystallization process. Hold the temperature at 55° C. for 2 h followed by 4 h at 45° C., then turn off the heat allowing the mixture to slowly reach 24° C. (RT). After stirring for 8 h with the heat off, cool the mixture to 0° C. for 2 hr, followed by 2 h at −10° C. Collect the resulting dense, white, granular crystals by vacuum filtration at −10° C. Rinse the crystals twice with cold (−10° C.) toluene and vacuum dry at 50° C., 5 Torr, for 12 hr, to give the title compound as a white solid (120.7 g, 99.5% purity, 88.8%).

1. temperatureHeat
2. dissolutionis dissolved
3. stirringstir the reaction mixture for 15 min at 70° C
4. customSeparate
5. washwash the organic layer with saturated aqueous sodium bicarbonate solution (2.00 L), brine (2.00 L)
6. dry with materialdry (sodium sulfate)
7. concentrationconcentrate
8. customa rotary evaporator at 70° C. until about 672.5 g
9. temperatureto maintain a vapor phase sufficient
10. customto prevent drying above the solvent line and self-seeding
11. customcrystallization under these conditions
12. temperatureUsing toluene heated to 70° C.
13. customto a preheated (70° C.) 3-neck flask
14. customequipped with a mechanical stirrer
15. waitLower the temperature to 58° C. over 1 h
16. customIf available, seed the solution with crystals of 7-chloro-6-hydroxy-3-(2,2,2-trifluoroacetyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine from a prior synthesis
17. customcrystallization
18. waitAfter 30 min
19. customfurther to 55° C.
20. customat 55° C.
21. customfor 2 h
22. waitfollowed by 4 h at 45° C.
23. customto slowly reach 24° C. (RT)
24. stirringAfter stirring for 8 h with the
25. temperatureheat off
26. temperaturecool the mixture to 0° C. for 2 hr
27. waitfollowed by 2 h at −10° C
28. customCollect the resulting dense, white, granular crystals
29. filtrationby vacuum filtration at −10° C
30. washRinse the crystals twice with cold (−10° C.) toluene and vacuum
31. customdry at 50° C.
32. wait5 Torr, for 12 hr

ORDレコード

ord-2ef1c64c6b424cf4954e0616b5abe15a

出典データセット

uspto-grants-2011_07

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07981882B2