반응 #2336112

ord-b404871d426a4fe08446e98aa1c72985

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The reaction mixture was evaporated to dryness
  2. 2
    기타the residue was triturated with ether (2×75 mL)
  3. 3
    workup.DISSOLUTIONThe ether insoluble solid was dissolved in water (15 mL)
  4. 4
    기타precipitated
  5. 5
    기타Crystallization of this material from water
  6. 6
    기타gave a colorless powder

실험 절차

A solution of 6 (0.75 g, 1 mmol) in methanol (75 mL) was adjusted to pH 9 with NaOCH3 and stirred at room temperature for 16 h. The reaction mixture was evaporated to dryness and the residue was triturated with ether (2×75 mL). The ether insoluble solid was dissolved in water (15 mL) and acidified with acetic acid whereupon the crude product precipitated. Crystallization of this material from water gave a colorless powder: yield 0.31 g, 78%: mp 238° C. (decomp.): UV λmax (pH 1) 215 nm (ε 2280), 245 (6900), 301 (8400): UV λmax (pH 7) 215 nm (ε 22,100), 245 (6900), 301 (8000): UV λmax (pH 11) 245 nm (ε 5700), 291 (6000). NMR (DMSO-d6) δ 5.79 (1H, d, J=5.32 Hz, C1, H), 6.90 (2H, s, NH2), 11.12 (1H, s, NH), and other sugar protons. Anal Calcd. for C10H12N4O6S.H2O: C, 35.92: H, 4.22: N, 16.76: S, 9.59. Found: C, 35.82: H, 4.02: N, 16.92: S, 9.66.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05041426uspto-grants-1991_08