Hydrochloric Acid → Cytidine, 2'-deoxy-5-methyl-, monohydrochloride

HRID 2416149ノート

反応式

HRID 2416149 の反応式
[Cl:1]C1C=CC(C([C@@:8]2([OH:33])[C@@H:12]([CH2:13][O:14]C(=O)C3C=CC(Cl)=CC=3)[O:11][C@@H:10]([N:24]3[CH:31]=[C:30]([CH3:32])[C:28]([NH2:29])=[N:27][C:25]3=[O:26])[CH2:9]2)=O)=CC=1.[OH-].[Na+].Cl>CO>[ClH:1].[CH3:32][C:30]1[C:28]([NH2:29])=[N:27][C:25](=[O:26])[N:24]([CH:31]=1)[C@@H:10]1[O:11][C@H:12]([CH2:13][OH:14])[C@@H:8]([OH:33])[CH2:9]1

参加物

5

反応条件

温度
45 °C

実験手順

To the suspension of 0.71 g of 3′,5′-O-bis(4-chlorobenzoyl)-5-methyl-2′-deoxycytidine in 4 mL of methanol was added 0.7 mL of the solution of sodium hydroxide in methanol (prepared by dissolving 100 mg of sodium hydroxide in 4 mL of methanol), and the mixture was heated at 45° C. for 5 hours with stirring. After cooling, the mixture was neutralized with a solution of hydrogen chloride in methanol, and methanol was evaporated off. After chloroform and water were added to the residue, the layers were separated, and the aqueous layer was washed with chloroform. The aqueous layer was concentrated and acidified with 6N aqueous hydrogen chloride solution, and after the addition of 5 mL of acetone, allowed to stand overnight at −14° C. The precipitated solid was filtered and dried to give 0.37 g of 5-methyl-2′-deoxycytidine hydrochloride as a light brown solid. Yield 97%.

後処理

  1. temperatureAfter cooling
  2. customwas evaporated off
  3. additionAfter chloroform and water were added to the residue
  4. customthe layers were separated
  5. washthe aqueous layer was washed with chloroform
  6. concentrationThe aqueous layer was concentrated
  7. additionafter the addition of 5 mL of acetone
  8. filtrationThe precipitated solid was filtered
  9. customdried

出典と根拠

ORDレコード
ord-3176068583324084bfbb4df18a6d428a
出典データセット
uspto-grants-2004_11
特許番号
US06822090B2

反応ノート

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