Pyrimidine → 4-amino-5-(4-phenoxyphenyl)-7-(3-tetrahydrofuryl)-7H-pyrrolo[2,3-d]pyrimidine

HRID 51522

反応式

HRID 51522 の反応式
[NH2:1][C:2]1[C:3]2[C:10]([C:11]3[CH:16]=[CH:15][C:14]([O:17][C:18]4[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=4)=[CH:13][CH:12]=3)=[CH:9][NH:8][C:4]=2[N:5]=[CH:6][N:7]=1.N1C=CC=NC=1.[H-].[Na+].[O:32]1[CH2:36][CH2:35][C@@H:34](C2C=C(S([O-])(=O)=O)C(C)=CC=2)[CH2:33]1>CN(C)C=O.C(OCC)(=O)C.C(N(CC)CC)C.CO>[NH2:1][C:2]1[C:3]2[C:10]([C:11]3[CH:12]=[CH:13][C:14]([O:17][C:18]4[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=4)=[CH:15][CH:16]=3)=[CH:9][N:8]([CH:34]3[CH2:35][CH2:36][O:32][CH2:33]3)[C:4]=2[N:5]=[CH:6][N:7]=1

参加物

7

反応物 4

HCID 9260PyrimidineHCID 24758Sodium hydrideHCID 120422345-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-ylamineHCID 865890094-{(S)-tetrahydrofuran-3-yl}toluenesulphonate

生成物 1

HCID 227363324-amino-5-(4-phenoxyphenyl)-7-(3-tetrahydrofuryl)-7H-pyrrolo[2,3-d]pyrimidine収率 75%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒3 回HCID 21980445Ethyl acetate methanol triethylamine溶媒

実験手順

To a stirred suspension of 4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidine (4.83 g, 16 mmol) in N,N-dimethylformamide (80 mL), under an d]pyrimidine (4.83 g, 16 mmol) in N,N-dimethylformamide (80 mL), under an atmosphere of nitrogen, was added 60% sodium hydride in mineral oil (0.75 g, 19 mmol), and the mixture stirred at room temperature for 30 minutes. The resultant dark solution was treated with a solution of 4-{(S)-tetrahydrofuran-3-yl}toluenesulphonate (4.20 g, 18 mmol) in N,N-dimethylformamide (20 mL) in 2 mL aliquots. The resultant solution was stirred at room temperature for 30 minutes, then at 95 deg. C. for 18 hours. The solution was allowed to cool to ambient temperature, then poured onto ice/water (200 mL). The aqueous was extracted with ethyl acetate (3×200 mL). The combined organic extracts were washed with water (4×150 mL), dried over sodium sulphate, and the solvent was removed under reduced pressure. The residue was warmed with dichloromethane (1000 mL) until a solution was obtained, cooled to ambient temperature, and purified by chromatography with a Biotage 40M column using ethyl acetate/triethylamine (95:5), then ethyl acetate/triethylamine/methanol (90:5:5) as a mobile phase, to yield R-(+)-4-[4-amino-5-(4-phenoxyphenyl)-7-(3-tetrahydrofuryl)-7H-pyrrolo[2,3-d]pyrimidine as an off-white solid (4.35 g, 12 mmol) melting point 165-166 deg. C., LC/MS: Hypersil BDS c18 (100×2.1 mm) 0.1M ammoniumacetate/acetonitrile, 10-100% acetonitrile in 8 min.) MH+373 tr=4.44 minutes. [ ]D+20.5±0.6 (dichloromethane, 22.6 deg. C.)

後処理

  1. customat 95 deg. C
  2. waitfor 18 hours
  3. temperatureto cool to ambient temperature
  4. additionpoured onto ice/water (200 mL)
  5. extractionThe aqueous was extracted with ethyl acetate (3×200 mL)
  6. washThe combined organic extracts were washed with water (4×150 mL)
  7. dry with materialdried over sodium sulphate
  8. customthe solvent was removed under reduced pressure
  9. temperatureThe residue was warmed with dichloromethane (1000 mL) until a solution
  10. customwas obtained
  11. temperaturecooled to ambient temperature
  12. custompurified by chromatography with a Biotage 40M column

出典と根拠

ORDレコード
ord-903ad30abb624097a446f3d9e2327406
出典データセット
uspto-grants-2004_03
特許番号
US06713474B2

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