Ethyl Acetate → HCID 44623470, compound

HRID 535703Notes

Reaction equation

HRID 535703 reaction equation
[Cl:1][C:2]1[N:7]=[C:6](Cl)[C:5]([NH2:9])=[CH:4][N:3]=1.OP([O-])([O-])=O.[K+].[K+].[C:17]([O:20][CH2:21][CH3:22])(=O)[CH3:18]>C(#N)C.O.C([O-])(=O)C.[Pd+2].C([O-])(=O)C.C1(P(C2CCCCC2)C2C=CC=CC=2C2C(OC)=CC=CC=2OC)CCCCC1>[Cl:1][C:2]1[N:7]=[C:6](/[CH:18]=[CH:17]/[O:20][CH2:21][CH3:22])[C:5]([NH2:9])=[CH:4][N:3]=1

Participants

8

Conditions

Temperature
80 °C

Procedure

A mixture of 2,4-dichloropyrimidin-5-amine (2.0 g, 12.2 mmol), product of Example 100G (6.04 g, 30.5 mmol), potassium phosphate dibasic (5.31 g, 30.5 mmol), palladium(II) acetate (0.027 g, 0.122 mmol) and dicyclohexyl-(2′,6′-dimethoxy-[1,1′-biphenyl]-2-yl)phosphine (0.050 g, 0.122 mmol) in acetonitrile (30 mL) and water (20 mL) under argon was refluxed at 80° C. for 16 h. The reaction mixture was cooled, diluted with ethyl acetate, and washed with water (2×30 mL) and saturated aqueous brine. The organic layer was dried over sodium sulfate and filtered. The filtrate was concentrated and purified by flash chromatography using 30% ethyl acetate in hexane to afford title compound (0.3 g, 12.32%) as an oil. 1H NMR (300 MHz, CDCl3): δ 7.89 (s, 1H), 7.85 (d, J=11.7 Hz, 1H), 5.69 (d, J=11.7 Hz, 1H), 4.05 (q, J=7.2 Hz, 2H), 3.49 (bs, 2H), 1.37 (t, J=7.5 Hz, 3H).

Workup

  1. temperatureThe reaction mixture was cooled
  2. washwashed with water (2×30 mL) and saturated aqueous brine
  3. dry with materialThe organic layer was dried over sodium sulfate
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated
  6. custompurified by flash chromatography

Sources & evidence

ORD record
ord-ad8d9f79174d4baebdecd0a3b480dc34
Source dataset
uspto-grants-2014_10
Patent number
US08859536B2

Reaction notes

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