Cesium carbonate → HCID 178493187, compound

HRID 2271820Notes

Reaction equation

HRID 2271820 reaction equation
Br[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][C:6]([C:12]([CH:14]1[CH2:16][CH2:15]1)=[O:13])=[C:5]2[NH:17][C@H:18]1[CH2:23][CH2:22][C@H:21]([CH2:24][N:25]2[CH2:29][CH2:28][CH:27]([O:30][CH3:31])[CH2:26]2)[CH2:20][CH2:19]1.[Cl:32][C:33]1[CH:38]=[C:37](B2OC(C)(C)C(C)(C)O2)[CH:36]=[C:35]([Cl:48])[C:34]=1[OH:49].C([O-])([O-])=O.[Cs+].[Cs+]>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]>[CH:14]1([C:12]([C:6]2[CH:7]=[N:8][C:9]3[C:4]([C:5]=2[NH:17][C@H:18]2[CH2:19][CH2:20][C@H:21]([CH2:24][N:25]4[CH2:29][CH2:28][CH:27]([O:30][CH3:31])[CH2:26]4)[CH2:22][CH2:23]2)=[CH:3][C:2]([C:37]2[CH:38]=[C:33]([Cl:32])[C:34]([OH:49])=[C:35]([Cl:48])[CH:36]=2)=[CH:11][CH:10]=3)=[O:13])[CH2:15][CH2:16]1

Participants

6

Reactant 3

HCID 10796Cesium carbonateHCID 667151272,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 178493186HCID 178493186, compound

Product 1

HCID 178493187HCID 178493187, compoundYield 54%

Reagents, catalysts & solvents 2

HCID 178418228Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)CatalystHCID 312751,4-DioxaneSolvent

Conditions

Temperature
80 °C

Procedure

To a suspension of (6-bromo-4-((trans-4-((3-methoxypyrrolidin-1-yl)methyl)cyclohexyl)amino)quinolin-3-yl)(cyclopropyl)methanone (49 mg, 0.10 mmol), 2,6-dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (43 mg, 0.15 mmol) and Pd(dppf)Cl2 (11 mg, 0.015 mmol) in dioxane (4 mL) was added Cs2CO3 (1.0 M in H2O, 0.4 mL, 0.4 mmol). N2 gas was bubbled through the reaction mixture and the mixture was then heated at 80° C. for 2 h. The solution was allowed to cool to room temperature, then directly subjected to column chromatography (silica, 0-20% methanol/dichloromethane). The resultant residue was dissolved in ethyl acetate and washed with saturated sodium bicarbonate solution. The organic layer was dried over anhydrous sodium sulfate and concentrated to afford the desired product (30.6 mg, 54%) as a yellow solid. 1H NMR (500 MHz, MeOD+TFA-d) δ 9.36 (br s, 1H), 8.47 (br s, 1H), 8.27 (dd, J=8.7, 1.8 Hz, 1H), 7.98 (d, J=8.7 Hz, 1H), 7.75-7.71 (s, 2H), 4.53-4.49 (br s, 1H), 4.19 (d, J=18.9 Hz, 1H), 3.85-3.74 (m, 2H), 3.35 (s, 3H), 3.28-3.26 (m, 1H), 3.25-3.12 (m, 3H), 2.84 (br s, 1H), 2.45-2.29 (m, 3H), 2.20-1.97 (m, 4H), 1.80-1.73 (m, 2H), 1.37-1.18 (m, 6H). ESI MS m/z 568 [C31H35Cl2N3O3+H]+; HPLC>99% (AUC), tR=11.42 min.

Workup

  1. customN2 gas was bubbled through the reaction mixture
  2. temperatureto cool to room temperature
  3. dissolutionThe resultant residue was dissolved in ethyl acetate
  4. washwashed with saturated sodium bicarbonate solution
  5. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-72f46ddf520a4dfeb97fd606390b8ffc
Source dataset
uspto-grants-2015_09
Patent number
US09120749B2

Reaction notes

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