Réaction #68663

Équation de réaction

5-bromo-3-methylisothiazole

isopropylmagnesium chloride

3,6-dichloropyridazine

3,6-dichloropyridazine

→

desired product

3-chloro-6-(3-methylisothiazol-5-yl)pyridazine

Solvants

THF

THF

THF

Conditions de réaction

Traitement

1. 1
   Températurethe reaction was heated to 50° C. for 16 hours
2. 2
   TempératureThe reaction was then cooled to 23° C.
3. 3
   Autrequenched with 60 mL of satd
4. 4
   workup.ADDITIONThe mixture was mixed with celite and 100 mL of EtOAc
5. 5
   AutreThe insoluble material was removed by filtration
6. 6
   workup.ADDITIONThe filtrate was diluted with 40 mL of EtOAc and 30 mL of water
7. 7
   AutreThe organic phase was separated
8. 8
   Lavagewashed with 60 mL of brine
9. 9
   Séchagedried over Na2SO4
10. 10
    Concentrationconcentrated in vacuo
11. 11
    AutreThe residue was purified by a silica gel column chromatography (10% to 80% hex/EtOAc)

Mode opératoire

To a solution of 5-bromo-3-methylisothiazole (2.42 g, 14 mmol) in 20 mL of THF at −45° C. was added isopropylmagnesium chloride (19 ml, 19 mmol) in THF (1 M). After 20 minutes, zinc(II) chloride (41 ml, 20 mmol) in THF (0.5 M) was added and the solution was warmed up to rt. 3,6-dichloropyridazine (2.4 g, 16 mmol), 3,6-dichloropyridazine (2.4 g, 16 mmol) and Q-Phos (2.5 g) were added and the reaction was heated to 50° C. for 16 hours. The reaction was then cooled to 23° C. and quenched with 60 mL of satd. NH4Cl aq. solution. The mixture was mixed with celite and 100 mL of EtOAc. The insoluble material was removed by filtration. The filtrate was diluted with 40 mL of EtOAc and 30 mL of water. The organic phase was separated and washed with 60 mL of brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (10% to 80% hex/EtOAc) to afford red solid as desired product. MS (ESI pos. ion) m/z: 212 (MH+). Calc'd exact mass for C8H6ClN3S: 211.

Source