Sodium Carbonate → HCID 10288404, compound

HRID 1880505Notes

Reaction equation

HRID 1880505 reaction equation
Br[C:2]1[CH:7]=[CH:6][C:5]([C@H:8]([NH:16][C@H:17]([C:22]([NH:24][CH2:25][C:26]#[N:27])=[O:23])[CH2:18][CH:19]([CH3:21])[CH3:20])[C:9]([F:15])([F:14])[C:10]([F:13])([F:12])[F:11])=[CH:4][CH:3]=1.[N:28]1[CH:33]=[CH:32][C:31](B(O)O)=[CH:30][CH:29]=1.C([O-])([O-])=O.[Na+].[Na+]>CN(C=O)C.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]>[C:26]([CH2:25][NH:24][C:22](=[O:23])[C@H:17]([CH2:18][CH:19]([CH3:21])[CH3:20])[NH:16][C@@H:8]([C:5]1[CH:6]=[CH:7][C:2]([C:31]2[CH:32]=[CH:33][N:28]=[CH:29][CH:30]=2)=[CH:3][CH:4]=1)[C:9]([F:15])([F:14])[C:10]([F:13])([F:12])[F:11])#[N:27]

Participants

6

Conditions

Temperature
95 °C

Procedure

To a solution of N2-[(1S)-1-(4-bromophenyl)-2,2,3,3,3-pentafluoropropyl]-N1-(cyanomethyl)-L-leucinamide (82 mg, 0.18 mmol), 4-pyridylboronic acid (30 mg, 0.24 mmol) and PdCl2(dppf) (14 mg, 0.02 mmol) in 2.5 mL DMF was added 2M Na2CO3 (0.25 mL). The mixture was heated to 95° C. for 2.5 h, then cooled and partitioned between aq. Na2CO3 and ether. The aqueous phase was washed with brine and dried over MgSO4. Purification by silica gel chromatography (65% to 95% ethyl acetate/hexanes gradient) provided the title compound.

Workup

  1. temperaturecooled
  2. custompartitioned between aq. Na2CO3 and ether
  3. washThe aqueous phase was washed with brine
  4. dry with materialdried over MgSO4
  5. customPurification by silica gel chromatography (65% to 95% ethyl acetate/hexanes gradient)

Sources & evidence

ORD record
ord-55829048042d4b6d8b7da166acff5ee2
Source dataset
uspto-grants-2012_11
Patent number
US08318748B2

Reaction notes

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