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Acetoacetic Acid → 2-Bromo-5,6-dichloro-1-(5-deoxy-beta-D-ribofuranosyl)-1H-benzimidazole

HRID 2227171
ノート
印刷プレビュー

反応式

HRID 2227171 の反応式
[Br:1][C:2]1[N:6]([C@@H:7]2[O:19][C@H:18]([CH3:20])[C@@H:13]([O:14]C(=O)C)[C@H:8]2[O:9]C(=O)C)[C:5]2[CH:21]=[C:22]([Cl:26])[C:23]([Cl:25])=[CH:24][C:4]=2[N:3]=1.C(=O)([O-])[O-].[Na+].[Na+].CC(CC(O)=O)=O>C(O)C.CO.O>[Br:1][C:2]1[N:6]([C@@H:7]2[O:19][C@H:18]([CH3:20])[C@@H:13]([OH:14])[C@H:8]2[OH:9])[C:5]2[CH:21]=[C:22]([Cl:26])[C:23]([Cl:25])=[CH:24][C:4]=2[N:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 96Acetoacetic AcidHCID 10340Sodium CarbonateHCID 699962602-Bromo-5,6-dichloro-1-(5-deoxy-2,3-di-O-acetyl-beta-D-ribofuranosyl)benzimidazole

生成物 1

HCID 5129192-Bromo-5,6-dichloro-1-(5-deoxy-beta-D-ribofuranosyl)-1H-benzimidazole収率 48%

試薬・触媒・溶媒 3

HCID 702Ethanol溶媒
HCID 887
Methanol
溶媒
HCID 962Water溶媒

実験手順

2-Bromo-5,6-dichloro-1-(2,3-di-O-acetyl-5deoxy-beta-D-ribofuranosyl)-1H-benzimidazole (7.70 g, 16.52 mmol) was dissolved in ethanol (100 mL) and methanol (100 mL). A solution of sodium carbonate (1.75 g, 16.52 mmol) in water (30 mL) was added to the diacetate solution. The resulting mixture was stirred at rt for 17 h. The reaction mixture was concentrated, dissolved in ethyl acetate (125 mL) and extracted with water (3×50 mL). The ethyl acetate layer was dried with magnesium sulfate (anhyd), filtered, and evaporated. The crude residue was purified on a silica gel column with 1:30 methanol:CH—2Cl2. The resulting product was further purified on a silica gel column with 1:2 ethyl acetate: hexanes, followed by 1:1 ethyl acetate:hexanes to give the title compound (3.00 g, 7.85 mmol, 48%); MS (El): m/z (rel. intensity) 405 (0.05, M++Na); 1H NMR (DMSO-d6) δ8.00 (s, 1H, Ar—H), 7.87 (s, 1H, Ar—H), 5.87 (d, 1H, OH, J=6.7 Hz), 5.53 (d, 1H, OH, J=6.2 Hz), 5.29 (d, 1H, CH, J=5.1 Hz), 4.52 (m, 1H, CH), 4.01 (m, 1H, CH), 3.91 (m, 1H, CH), 1.42 (d, 3H, CH3, J=6.5 Hz).

後処理

  1. concentrationThe reaction mixture was concentrated
  2. dissolutiondissolved in ethyl acetate (125 mL)
  3. extractionextracted with water (3×50 mL)
  4. dry with materialThe ethyl acetate layer was dried with magnesium sulfate (anhyd)
  5. filtrationfiltered
  6. customevaporated
  7. customThe crude residue was purified on a silica gel column with 1:30 methanol
  8. customThe resulting product was further purified on a silica gel column with 1:2 ethyl acetate

出典と根拠

ORDレコード
ord-93139f25358c4f18b48c226fd94ad7df
出典データセット
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06413938B1

反応ノート

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