Potassium Carbonate → HCID 135979606, compound

HRID 605998Notes

Reaction equation

HRID 605998 reaction equation
[CH2:1]([O:3][C:4](=[O:29])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([N:11]([C:19]2[C:20]3[N:21]([N:26]=[CH:27][N:28]=3)[C:22](Br)=[CH:23][N:24]=2)[C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])[CH:6]=1)[CH3:2].CC1(C)C(C)(C)OB([C:38]2[CH:39]=[N:40][NH:41][CH:42]=2)O1.C([O-])([O-])=O.[K+].[K+]>O1CCOCC1.O>[CH2:1]([O:3][C:4](=[O:29])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([N:11]([C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])[C:19]2[C:20]3[N:21]([N:26]=[CH:27][N:28]=3)[C:22]([C:38]3[CH:39]=[N:40][NH:41][CH:42]=3)=[CH:23][N:24]=2)[CH:6]=1)[CH3:2]

Participants

6

Conditions

Temperature
115 °C

Procedure

Nitrogen is bubbled through a mixture of 3-[(5-bromo-[1,2,4]triazolo[1,5-a]pyrazin-8-yl)-tert-butoxycarbonyl-amino]benzoic acid ethyl ester (0.58 g, 1.25 mmol), 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyrazole (0.49 g, 2.50 mmol), K2CO3 (0.35 g, 2.50 mmol) and Pd(dppf)Cl2DCM (102 mg, 0.125 mmol) in dioxane (37.5 mL) and water (9.6 mL). A condenser is fitted to the flask, the system is evacuated and purged with N2 (g) and then heated at 115° C. for 25 min. The heating bath is removed and CO2 (s) is added to cool and buffer the system. The solvent is removed under reduced pressure and the residue is purified by silica chromatography, eluting with 10% to 50% ethyl acetate in DCM, to afford the title compound as an orange oil (0.61 g, >100%) which is used without further purification.

Workup

  1. customA condenser is fitted to the flask
  2. customthe system is evacuated
  3. custompurged with N2 (g)
  4. customThe heating bath is removed
  5. additionCO2 (s) is added
  6. temperatureto cool
  7. customThe solvent is removed under reduced pressure
  8. customthe residue is purified by silica chromatography
  9. washeluting with 10% to 50% ethyl acetate in DCM

Sources & evidence

ORD record
ord-d4a62eca3f8c4d2caa06483678c4cfaf
Source dataset
uspto-grants-2011_03
Patent number
US07915256B2

Reaction notes

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