Ammonia → (2R,3R,4S,5R)-2-(2-amino-5,6-dichloro-benzimidazol-1-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol

HRID 1900117

反応式

HRID 1900117 の反応式
Cl[C:2]1[N:6]([C@@H:7]2[O:19][C@H:18]([CH2:20][O:21]C(=O)C)[C@@H:13]([O:14]C(=O)C)[C@H:8]2[O:9]C(=O)C)[C:5]2[CH:25]=[C:26]([Cl:30])[C:27]([Cl:29])=[CH:28][C:4]=2[N:3]=1.[NH3:31]>CO>[NH2:31][C:2]1[N:6]([C@@H:7]2[O:19][C@H:18]([CH2:20][OH:21])[C@@H:13]([OH:14])[C@H:8]2[OH:9])[C:5]2[CH:25]=[C:26]([Cl:30])[C:27]([Cl:29])=[CH:28][C:4]=2[N:3]=1

参加物

4

実験手順

2,5,6-Trichloro-1-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)benzimidazole (42, 0.48 g; I mmole) was dissolved in dry MeOH (10 ml). Liq. NH3 (10 ml) was added and the mixture heated in a steel bomb at 100° C. for 2 hr. This mixture was stirred at room temperature for 24 hr. Excess NH3 was allowed to evaporate and the solution evaporated to dryness, absorbed onto silica gel (2 g), and chromatographed on a silica gel column using silica gel (20 g; 60-200 mesh). Elution of the column with CH2Cl2 :CH3OH (96:4) gave the desired compound 44 as the major nucleoside. Evaporation of the solvent and crystallization of the residue from EtOH gave 44 (0.02 g; yield 6.08%). mp. 145° C.; UV Imax. (MeOH): 259 (7941) and 301 (8348) nm; Imax (pH1): 215 (26000) and 292 (7520) nm; Imax (pH11): 257 (7967) and 298 (7107) nm. 1H NMR(DMSO-d6): d 8.70 (s,1H, C7 -H, 8.28(s,1H, C4-H), 7.90 (bs,2H, D2O exchangeable, NH2), 6.75(d,C1'H, J1,2 =4.5 Hz) and the rest of the sugar protons.

後処理

  1. customto evaporate
  2. customthe solution evaporated to dryness
  3. customabsorbed onto silica gel (2 g)
  4. customchromatographed on a silica gel column
  5. washElution of the column with CH2Cl2 :CH3OH (96:4)

出典と根拠

ORDレコード
ord-e708a6bee24d4b2da94637a39be62386
出典データセット
uspto-grants-1996_11
特許番号
US05574058

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