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Dichloromethane → 2-(3,4-Dimethoxyphenyl)-5-(5-methoxypyridin-3-yl)imidazo[2,1-b][1,3,4]thiadiazole

HRID 2409563
Notes
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Reaction equation

HRID 2409563 reaction equation
Br[C:2]1[S:6][C:5]2=[N:7][CH:8]=[C:9](I)[N:4]2[N:3]=1.[CH3:11][O:12][C:13]1[CH:14]=[C:15](B(O)O)[CH:16]=[CH:17][C:18]=1[O:19][CH3:20].C([O-])([O-])=O.[K+].[K+].C(Cl)Cl.[CH3:33][O:34][C:35]1[CH:36]=[N:37][CH:38]=[C:39](B2OC(C)(C)C(C)(C)O2)[CH:40]=1>O1CCOCC1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[CH3:11][O:12][C:13]1[CH:14]=[C:15]([C:2]2[S:6][C:5]3=[N:7][CH:8]=[C:9]([C:39]4[CH:38]=[N:37][CH:36]=[C:35]([O:34][CH3:33])[CH:40]=4)[N:4]3[N:3]=2)[CH:16]=[CH:17][C:18]=1[O:19][CH3:20]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 5

HCID 6344Dichloromethane2×HCID 11430Potassium Carbonate2×HCID 27347023,4-Dimethoxyphenylboronic acidHCID 38661613-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridineHCID 662215402-Bromo-5-iodoimidazo[2,1-b][1,3,4]thiadiazole

Product 1

HCID 46940946
2-(3,4-Dimethoxyphenyl)-5-(5-methoxypyridin-3-yl)imidazo[2,1-b][1,3,4]thiadiazole

Reagents, catalysts & solvents 2

HCID 44119782Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)CatalystHCID 312751,4-DioxaneSolvent

Conditions

Temperature
110 °C

Procedure

2-bromo-5-iodoimidazo[2,1-b][1,3,4]thiadiazole (0.20 g, 0.606 mmol, 1 eq) was dissolved in dioxane (4 mL), and 3,4-dimethoxyphenylboronic acid was added (0.121 g, 0.667 mmol, 1.1 eq) followed by a saturated solution of K2CO3 (1 mL). The suspension was degassed (N2, 10 min), and Pd(dppf)Cl2.DCM (0.085 g, 0.121 mmol, 0.2 eq) was added. The mixture was heated in a nitrogen atmosphere at 110° C. for 2 h, when complete conversion was observed by LC-MS. 3-methoxypyridine-5-boronic acid pinacol ester was added (0.284 g, 1.21 mmol, 2 eq) followed by Pd(dppf)Cl2.DCM (0.085 g, 0.121 mmol, 0.2 eq) and a saturated solution of K2CO3 (1 mL). The mixture was stirred in a microwave oven (120° C., 30 min), cooled to RT and concentrated. The residue was taken up in AcOEt and n-BuOH and washed with water. The organic phase was separated, dried (Na2SO4), filtered and concentrated, and the crude was purified by flash chromatography (SiO2, DCM/EtOAc) and, subsequently, by preparative HPLC (RP-C18, ACN/water) to give the desired product. HPLC-MS (10-95% B in 4 min at 0.5 mL+2 min 100% B, flow 0.8 mL/min, 50° C.): tR=4.09 min, [M+H]+ m/z 369.1; 1H-NMR (DMSO-d6): δ=8.82 (1H, d, J=1.5 Hz), 8.21 (1H, d, J=2.7 Hz), 7.99 (1H, dd, J=2.7, 1.5 Hz), 7.94 (1H, s), 7.52 (1H, dd, J=8.4, 2.1 Hz), 7.46 (1H, d, J=2.1 Hz), 7.12 (1H, d, J=8.4 Hz), 3.88 (3H, s), 3.83 (3H, s), 3.81 (3H, s) ppm.

Workup

  1. customThe suspension was degassed (N2, 10 min), and Pd(dppf)Cl2
  2. temperaturecooled to RT
  3. concentrationconcentrated
  4. washn-BuOH and washed with water
  5. customThe organic phase was separated
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customthe crude was purified by flash chromatography (SiO2, DCM/EtOAc)

Sources & evidence

ORD record
ord-3da11d1d0ff44f68b08911a16fe948f9
Source dataset
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08815918B2

Reaction notes

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