Réaction #59660

Équation de réaction

sodium tert-butoxide

4-Chloro-1-(2-fluoro-4-methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidine

4-chloro-1-(2-fluoro-4-methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidine

carbamate

4-hydroxy-piperidine-1-carboxylic acid isopropyl ester

4-Hydroxy-Piperidine-1-Carboxylic Acid Isopropyl Ester

→

product ( 6 )

Rendement 74.4%

4-[1-(2-Fluoro-4-methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yloxy]-piperidine-1-carboxylic acid isopropyl ester

Rendement 74.4%

Solvants

Toluene

Conditions de réaction

Traitement

1. 1
   Autrereaction vessel
2. 2
   Autrefitted with a mechanical stirrer, nitrogen inlet
3. 3
   Autrea slurry was obtained
4. 4
   workup.STIRRINGwith stirring
5. 5
   TempératureThe internal temperature gradually increased to 34° C. due to an exotherm
6. 6
   Autrewas brought down to 23-25° C
7. 7
   workup.STIRRINGwas stirred at room temperature for 2.5 h
8. 8
   FiltrationThe precipitate from the reaction mixture was filtered
9. 9
   Lavagewashed with toluene (250 mL)
10. 10
    Autredried overnight at room temperature
11. 11
    Autrewas slurried in EtOH (500 mL) at room temperature
12. 12
    Filtrationfiltered
13. 13
    Lavagewashed with water (2.5 L) until the filtrate
14. 14
    workup.DISSOLUTIONThe washed solid product was dissolved
15. 15
    Températurein refluxing EtOH (1.3 L)
16. 16
    Températurethe resulting clear solution was gradually cooled to room temperature
17. 17
    AutreThe product (6) crystallized out and
18. 18
    Autrewas isolated by filtration
19. 19
    Autredried overnight in a vacuum oven at 40° C.

Mode opératoire

Toluene (1.6 L) was transferred to a 4 L jacketed reaction vessel fitted with a mechanical stirrer, nitrogen inlet and a temperature probe. 4-Chloro-1-(2-fluoro-4-methanesulfonyl-phenyl)-1H-pyrazolo[3,4-d]pyrimidine (7) (97.0 g, 0.297 mol) was added with stirring into the reaction vessel under nitrogen, and a slurry was obtained. The carbamate, 4-hydroxy-piperidine-1-carboxylic acid isopropyl ester (5) (66.57 g, 0.356 mol), was added at room temperature. The reactor was cooled to 12° C. and sodium tert-butoxide (37.09 g, 0.386 mol) was added with stirring. The internal temperature gradually increased to 34° C. due to an exotherm. Then the internal temperature was brought down to 23-25° C. The reaction mixture became a thick slurry and was stirred at room temperature for 2.5 h. The precipitate from the reaction mixture was filtered, washed with toluene (250 mL) followed by water (3×500 mL), and vacuum dried overnight at room temperature. The dried solid product was slurried in EtOH (500 mL) at room temperature, filtered, and washed with water (2.5 L) until the filtrate was neutral. The washed solid product was dissolved in refluxing EtOH (1.3 L), and the resulting clear solution was gradually cooled to room temperature. The product (6) crystallized out and was isolated by filtration and dried overnight in a vacuum oven at 40° C., 20 torr to provide 105.5 g of product (6) (74%). HPLC analysis, >99% (purity, by peak area). 1H NMR (Bruker 400 MHz, CDCl3) δ 8.62 (s, 1H, Ar—H), 8.32 (s, 1H, Ar—H), 7.93 (m, 3H, Ar—H), 5.62 (m, 1H, —O—CH—), 4.95 (m, 1H, CH3—CH—CH3), 3.91 (m, 2H, —CH2—), 3.37 (m, 2H, —CH2—), 3.12 (s, 3H, —SO2CH3), 2.09 (m, 2H, —CH2—), 1.87 (m, 2H, —CH2—), 1.27 (d, 6H, J=8 Hz, CH3—CH—CH3); mass spec. (electrospray) m/z 478 (M+H).

Source