反応 #635720

ord-9d0241779ead487bba98d851078ae6c1

反応方程式

Cl.N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O
D-Glucosamine hydrochloride
C[O-].[Na+]
sodium methoxide
CCN(C(C)C)C(C)C
diisopropylethylamine
O=CC[C@@H](O)[C@H](O)[C@H](O)CO
2-deoxyglucose

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGThe resulting solution was stirred under argon atmosphere for 20 hrs
  2. 2
    その他After removing solvent and base by vacuum
  3. 3
    その他the crude obtained
  4. 4
    洗浄was washed with both CH2Cl2 and, water
  5. 5
    その他subsequently crystallized from MeOH

実験手順

D-Glucosamine hydrochloride (13 mg, 0.06 mmol) was added to a solution containing sodium methoxide (3.24 mg, 0.06 mmol) in 3 mL DMSO. The reaction mixture was stirred at room temperature for 2 hrs, and purpurin-18-N-3′-(isothiocyanate)propylimide (19 mg, 0.028 mmol) and 50 μL diisopropylethylamine were added. The resulting solution was stirred under argon atmosphere for 20 hrs. After removing solvent and base by vacuum, the crude obtained was washed with both CH2Cl2 and, water and subsequently crystallized from MeOH. The desired 2-deoxyglucose conjugate (5) was obtained (8 mg). The filtrate was further concentrated and purified by silica gel plate chromatography (10% MeOH in CH2Cl2) to yield 4 mg of product. Thus, the total yield for 5 was 50% (12 mg). UV-vis in DMSO λmax: 366 nm (ε: 5.3×105), 419 (1.4×104), 550 (2.4×104), 648 (8.0×103) and 705 (5.2×104). Mass calcd for C44H53N7O9S: 878.3523 (M+Na)+; found by HRMS; 878.3542 (M+Na)+. 1H NMR (DMSO-d-6, δ ppm): 9.27, 9.16 and 8.85 (each s, 1H, for 10, 5 and 20-H), 8.01 (dd, 1H), 7.80 (br, 1H), 6.55 (br, 1H), 6.33 (d, 1H), 6.12 (d, 1H), 5.24-4.21 (9H), 3.80-3.40 (13H), 2.90 (s, 3H), 2.60 (m, 1H), 2.50-2.30 (m, 2H), 2.08 (m, 2H), 1.8 (m, 1H), 1.72 (d, 3H), 1.41 (t, 3H), −0.61 and −0.67 (each s, 1H, 2×NH).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07943586B2uspto-grants-2011_05