Sodium Carbonate → 6-{[6-(2-Methoxyphenyl)-5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4-yl]amino}hexanoic acid methyl ester

HRID 1926951Notes

Reaction equation

HRID 1926951 reaction equation
C(=O)([O-])[O-].[Na+].[Na+].[CH3:7][O:8][C:9](=[O:34])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][NH:15][C:16]1[C:17]2[C:24]([C:25]3[CH:30]=[CH:29][C:28]([O:31][CH3:32])=[CH:27][CH:26]=3)=[C:23](Br)[O:22][C:18]=2[N:19]=[CH:20][N:21]=1.[CH3:35][O:36][C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][C:38]=1B(O)O>CS(C)=O.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>[CH3:7][O:8][C:9](=[O:34])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][NH:15][C:16]1[C:17]2[C:24]([C:25]3[CH:30]=[CH:29][C:28]([O:31][CH3:32])=[CH:27][CH:26]=3)=[C:23]([C:38]3[CH:39]=[CH:40][CH:41]=[CH:42][C:37]=3[O:36][CH3:35])[O:22][C:18]=2[N:19]=[CH:20][N:21]=1

Participants

6

Conditions

Temperature
80 °C

Procedure

Add 0.45 ml of a 2 M aqueous sodium carbonate solution to a mixture of 200 mg (0.45 mmol) 6-{[6-bromo-5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4-yl]amino}hexanoic acid methyl ester and 16 mg (0.02 mmol) bis(triphenylphosphine)palladium(II) chloride in 10 ml dimethylsulphoxide. Next, add 85 mg (0.56 mmol) (2-methoxyphenyl)boronic acid and stir the mixture for 15 h at 80° C. Filter the reaction mixture and purify directly by preparative RP-HPLC (gradient: water/acetonitrile). 63 mg (42% of theor.) of the desired product is obtained.

Workup

  1. filtrationFilter the reaction mixture
  2. custompurify directly by preparative RP-HPLC (gradient: water/acetonitrile)

Sources & evidence

ORD record
ord-efda39feff1e41419cb5b13757a67028
Source dataset
uspto-grants-2012_05
Patent number
US08183246B2

Reaction notes

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