HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Dimethylformamide → 6-(2,4-Difluorophenyl)-5-(3-isopropyl-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)imidazo[2,1-b]thiazole

HRID 1930046
Notes
Print preview

Reaction equation

HRID 1930046 reaction equation
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9]1[N:10]=[C:11]2[N:15]([C:16]=1I)[CH:14]=[CH:13][S:12]2.C([Mg]Cl)(C)C.I[C:24]1[CH:25]=[CH:26][C:27]2[N:28]([C:30]([CH:33]([CH3:35])[CH3:34])=[N:31][N:32]=2)[N:29]=1.CN(C=O)C>C1COCC1.O.[Cl-].[Cl-].[Zn+2].C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.[O-]S([O-])(=O)=O.[Zn+2]>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9]1[N:10]=[C:11]2[N:15]([C:16]=1[C:24]1[CH:25]=[CH:26][C:27]3[N:28]([C:30]([CH:33]([CH3:35])[CH3:34])=[N:31][N:32]=3)[N:29]=1)[CH:14]=[CH:13][S:12]2
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

10

Reactant 4

HCID 6228DimethylformamideHCID 579298936-Iodo-3-isopropyl-[1,2,4]triazolo[4,3-b]pyridazineHCID 594578306-(2,4-Difluorophenyl)-5-iodoimidazo[2,1-b]thiazoleHCID 178418918HCID 178418918, compound

Product 1

HCID 579299526-(2,4-Difluorophenyl)-5-(3-isopropyl-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)imidazo[2,1-b]thiazoleYield 23%

Reagents, catalysts & solvents 5

HCID 24424Zinc SulfateCatalystHCID 3007855ZincchlorideCatalystHCID 178418397HCID 178418397, compoundCatalystHCID 962WaterSolventHCID 8028TetrahydrofuranSolvent2×

Conditions

Temperature
-30 °C

Procedure

The 6-(2,4-difluorophenyl)-5-iodoimidazo[2,1-b]thiazole (1.00 g, 2.76 mmol) was suspended in THF (7.5 mL) then cooled to about −30° C. The i-PrMgCl (2 M in THF, 1.52 mL, 3.04 mmol) was added dropwise over about 15 min then stirred at about −30° C. for about 15 min. The ZnCl2 (0.489 g, 3.59 mmol) was dissolved in THF (7.5 mL), cooled to about 0° C., and added dropwise to the Grignard solution. The reaction mixture was stirred for about 30 min at about −30° C. The 6-iodo-3-isopropyl-[1,2,4]triazolo[4,3-b]pyridazine (0.796 g, 2.76 mmol) was added to DMF (7.50 mL) and heated to about 80° C. to dissolve the material. Pd(Ph3P)4 (0.128 g, 0.110 mmol) was then added to the solution and the mixture was immediately added to the zincate suspension. The mixture was immediately heated to about 55° C. for about 45 min, then cooled, diluted with water and extracted with EtOAc. The organic solution was dried over MgSO4, filtered, and concentrated under reduced pressure. Purification by flash chromatography on silica gel with DCM/MeOH (95:5) followed by trituration with MeOH (5 mL) gave a solid that was collected by filtration. The filtrate was concentrated under reduced pressure then purified by RP-HPLC using (Table 1, Method d). The desired fractions were concentrated under reduced pressure to give a solid that was collected by filtration. The two crops were combined to give the title compound (0.250 g, 23%): LC/MS (Table 1, Method a) Rt=2.46 min; MS m/z: 397.2 (M+H)+.

Workup

  1. temperaturecooled to about 0° C.
  2. additionadded dropwise to the Grignard solution
  3. stirringThe reaction mixture was stirred for about 30 min at about −30° C
  4. temperatureheated to about 80° C.
  5. dissolutionto dissolve the material
  6. temperatureThe mixture was immediately heated to about 55° C. for about 45 min
  7. temperaturecooled
  8. extractionextracted with EtOAc
  9. dry with materialThe organic solution was dried over MgSO4
  10. filtrationfiltered
  11. concentrationconcentrated under reduced pressure
  12. customPurification by flash chromatography on silica gel with DCM/MeOH (95:5)
  13. customgave a solid
  14. filtrationthat was collected by filtration
  15. concentrationThe filtrate was concentrated under reduced pressure
  16. customthen purified
  17. concentrationThe desired fractions were concentrated under reduced pressure
  18. customto give a solid
  19. filtrationthat was collected by filtration

Sources & evidence

ORD record
ord-eebc897e489548fa9a57557bc35c05b7
Source dataset
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08188083B2

Reaction notes

Loading…

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes