Potassium Carbonate → HCID 14306333, compound

HRID 728801Notes

Reaction equation

HRID 728801 reaction equation
[NH2:1][C:2]1[N:10]=[C:9]2[C:5]([NH:6][CH:7]=[N:8]2)=[C:4]([Cl:11])[N:3]=1.C(=O)([O-])[O-].[K+].[K+].[CH:18]1[S:22][CH:21]=[CH:20][C:19]=1CBr.CO.[CH2:27](Cl)Cl>CN(C=O)C>[NH2:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[CH2:27][C:18]2[S:22][CH:21]=[CH:20][CH:19]=2)=[C:4]([Cl:11])[N:3]=1

Participants

6

Reactant 4

HCID 11430Potassium CarbonateHCID 5207033-(Bromomethyl)thiopheneHCID 53603492-Amino-6-chloropurineHCID 21226129Dichloromethane methanol

Product 1

HCID 14306333HCID 14306333, compound

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

A mixture of 2-amino-6-chloropurine (Aldrich Chemical Co.) (7.47 g; 0.44 mol), potassium carbonate (6.64 g; 0.048 mol), and 3-thenylbromide (see U.S. Pat. No. 3,746,724) (7.8 g; 0.044 mol) in DMF (200 ml) was stirred under nitrogen at room temperature for 48 hours. The mixture was filtered and the filtrate evaporated to dryness under vacuum, ethyl ether was addedand the precipitate was collected by filtration to give a mixture of 7- and9-substituted chloropurines. A sample of pure 9isomer was prepared by chromatography on silica gel with 5% methanol/methylene chloride as the eluting solvent to separate it from the 7-isomer. Analytical sample was obtained by crystallization from acetonemethanol mixture, yield 2.36 g, mpsoftens at 185° C. (dec) and then melts at 203°-204° C. (dec).

Workup

  1. filtrationThe mixture was filtered
  2. customthe filtrate evaporated to dryness under vacuum, ethyl ether
  3. filtrationwas collected by filtration
  4. customto give
  5. customto separate it from the 7-isomer
  6. customAnalytical sample was obtained by crystallization from acetonemethanol mixture, yield 2.36 g

Sources & evidence

ORD record
ord-b1b9522c44fc467198a6d779c091e039
Source dataset
uspto-grants-1991_09
Patent number
US05051429

Reaction notes

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