Cesium carbonate → HCID 67232888, compound

HRID 2035642Notes

Reaction equation

HRID 2035642 reaction equation
Cl[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[C:5]([F:12])[CH:6]=[CH:7][CH:8]=2)[N:3]=1.[N:13]1[N:14]=[CH:15][N:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=12.C([O-])([O-])=O.[Cs+].[Cs+]>O1CCOCC1.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[N:13]1[N:14]=[C:15]([C:2]2[CH:11]=[CH:10][C:9]3[C:4](=[C:5]([F:12])[CH:6]=[CH:7][CH:8]=3)[N:3]=2)[N:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=12

Participants

6

Procedure

2-Chloro-8-fluoroquinoline (0.75 g, 4.13 mmol) was combined with [1,2,4]triazolo[4,3-a]pyridine (0.541 g, 4.54 mmol), micronized Cs2CO3 (2.69 g, 8.26 mmol), and PdCl2(PPh3)2 (0.290 g, 0.413 mmol) then the mixture was slurried in dioxane (20 mL). The reaction was deoxygenated with argon and heated to reflux for 20 hours, then cooled, diluted with CHCl3 and filtered through a pad of Celite®. The filtrate was concentrated onto Na2SO4 powder (15 g) and the mixture was chromatographed on SiO2 eluting with a stepped gradient of 0-2% MeOH/ethyl acetate. The desired product was isolated as a cream-colored solid (1.12 g). MS APCI (+) m/z 265.3 (M+1) detected.

Workup

  1. customThe reaction was deoxygenated with argon
  2. temperatureheated
  3. temperatureto reflux for 20 hours
  4. temperaturecooled
  5. additiondiluted with CHCl3
  6. filtrationfiltered through a pad of Celite®
  7. concentrationThe filtrate was concentrated onto Na2SO4 powder (15 g)
  8. customthe mixture was chromatographed on SiO2 eluting with a stepped gradient of 0-2% MeOH/ethyl acetate

Sources & evidence

ORD record
ord-2fae27353f90403a8fe4c3ee52c23512
Source dataset
uspto-grants-2013_11
Patent number
US08575145B2

Reaction notes

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