Thymidine → HCID 18649770、化合物

HRID 2081784ノート

反応式

HRID 2081784 の反応式
[CH:1]1([CH2:4][NH:5][C:6]2[N:14]=[CH:13][N:12]=[C:11]3[C:7]=2[NH:8][CH:9]=[N:10]3)[CH2:3][CH2:2]1.[C@@H:15]1(N2C=C(C)C(=O)NC2=O)[O:21][C@H:18]([CH2:19][OH:20])[CH2:17][CH2:16]1.P([O-])([O-])([O-])=O.[K+].[K+].[K+].[N-]=[N+]=[N-].[K+].[C@@H]1(N2C=C(C)C(=O)NC2=O)O[C@H](CO)[C@@H](O)C1>CN(C)C=O>[CH:1]1([CH2:4][NH:5][C:6]2[N:14]=[CH:13][N:12]=[C:11]3[C:7]=2[NH:8][CH:9]=[N:10]3)[CH2:2][CH2:3]1.[CH:1]1([CH2:4][NH:5][C:6]2[N:14]=[CH:13][N:12]=[C:11]3[C:7]=2[N:8]=[CH:9][N:10]3[C@H:15]2[CH2:16][CH2:17][C@@H:18]([CH2:19][OH:20])[O:21]2)[CH2:2][CH2:3]1

参加物

8

反応物 5

HCID 5789ThymidineHCID 62657Potassium Phosphate, TribasicHCID 651192',3'-DideoxythymidineHCID 3362547N-(Cyclopropylmethyl)adenineHCID 10290740Potassium azide

生成物 2

HCID 3362547N-(Cyclopropylmethyl)adenineHCID 18649770HCID 18649770、化合物収率 154%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
35 °C

実験手順

6-(Cyclopropylmethylamino)purine was prepared by nucleophilic displacement of the chlorine group on 6-chloropurine (Sigma Chemicals. St. Louis, Mo.) by the amino group on cyclopropylmethylamine (Karl Industries, Aurora, Ohio). 6-(Cyclopropylmethylamino)purine (2.64 mmol, 0.50 g) was dissolved in 5 mL of dimethylformamide with heating. After cooling to room temperature 3'-deoxythymidine (3.98 mmol, 0.90 g) (Horwitz J. P. et al., J. Org. Chem. 31, 205 (1966)) was added along with 30 mL of 10 mM potassium phosphate buffer with a pH of 6.8 containing 0.04% potassium azide. Purified thymidine phosphorylase (10,000 I.U.) and purine nucleoside phosphorylase (20,000 I. U.) (Krenitsky T. A. et al., Biochemistry 20, 3615, 1981 and U.S. Pat. No. 4,381,4440 absorbed onto 10 mL DEAE cellulose (Whatman) were added, and the suspension was stirred at 35° C. After 8 hours the reaction was filtered, and the filtrate was applied to a series of coupled columns. The initial column contained AG1-X 2 resin (OH form), 2.5×10 cm, while the second column contained Amberlite XAD-2 resin, 2.5×20 cm. After sample application, the columns were washed with 500 mL water and the product was eluted with methanol. The product was then flash chromatographed on a silica gel column, 5×20 cm, with a mixture of chloroform:methanol (9:1, v/v). Solvent was removed in vacuo and the product gum was transferred in acetone to a vial. Lyophilization yielded 0.588 g of 6-(cyclopropylmethylamino)-9-((2R,5S)-tetrahydro-5-(hydroxymethyl)-2-furyl)-9H-purine, that analysed for 0.15 water and 0.15 acetone.

後処理

  1. temperaturewith heating
  2. custom4,381,4440 absorbed onto 10 mL DEAE cellulose (Whatman)
  3. additionwere added
  4. filtrationAfter 8 hours the reaction was filtered
  5. washAfter sample application, the columns were washed with 500 mL water
  6. washthe product was eluted with methanol
  7. customflash chromatographed on a silica gel column, 5×20 cm, with a mixture of chloroform:methanol (9:1
  8. customSolvent was removed in vacuo

出典と根拠

ORDレコード
ord-2749df9807fa41829b4799669e827190
出典データセット
uspto-grants-1993_02
特許番号
US05185437

反応ノート

読み込み中…