반응 #1951030

ord-e7dcb4dcab15404bbfffedb092d36555

반응 방정식

N#Cc1c(Cl)n([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c2cc(Cl)c(Cl)cc12
2,5,6-Trichloro-3-cyano-1-(β-D-ribofuranosyl)indole
NN.O
hydrazine hydrate
Nc1n[nH]c2c1c1cc(Cl)c(Cl)cc1n2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
4.37
수율 90.0%
Nc1n[nH]c2c1c1cc(Cl)c(Cl)cc1n2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
5,6-Dichloro-3-amino-8-(β-D-ribofuranosyl)pyrazolo[3,4-b]indole
수율 90.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The suspension thus obtained
  2. 2
    온도cooled to 0° C.
  3. 3
    여과the suspension filtered
  4. 4
    세척the solids rinsed with water
  5. 5
    기타The solids were recrystallized from MeOH/H2O

실험 절차

2,5,6-Trichloro-3-cyano-1-(β-D-ribofuranosyl)indole (4.4, 102 mg, 0.27 mmol) was dissolved in hydrazine hydrate (2 mL), and the resulting solution was stirred at room temperature for 30 min. The suspension thus obtained was diluted with water (8 mL), cooled to 0° C., and the suspension filtered and the solids rinsed with water. The solids were recrystallized from MeOH/H2O to yield 91 mg (90%) of 4.37 as a white crystalline solid: mp 198-201° C.; Rf0.3 (20% MeOH/CHCl3); 1H-NMR (500 MHz, DMSO-d6): δ 8.68 (s, 1H, D2O exch.), 7.76 (s, 1H), 7.27 (s, 1H), 5.81 (d, 1H), 5.78 (b, 1H, D2O exch.), 5.31-5.28 (m, 2H, D2O exch.), 4.84 (s, 2H, D2O exch.), 4.27 (q, 1H), 4.07 (s, 1H), 4.00 (s, 1H), 3.68 (q, 2H). 13C-NMR (125 MHz, DMSO-d6): δ 155.50, 131.99, 129.00, 123.60, 121.60, 116.91, 115.45, 111.96, 88.32, 85.95, 71.06, 69.95, 63.28, 60.78. HRMS (EI) m/z calcd. for C14H14Cl2N4O4 372.0392, found 372.0397. Anal calcd for C14H14Cl2N4O4.¼H2O: C, 44.52; H, 3.87; N, 14.83. Found: C, 44.63; H, 4.10; N, 14.72.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07625871B2uspto-grants-2009_12