تفاعل #1951037

ord-91d27921d0d742f1b597f515d372be73

معادلة التفاعل

CC(=O)OC[C@H]1O[C@@H](n2c(Br)c(C=O)c3cc(Cl)c(Cl)cc32)[C@H](O)[C@@H]1O
5,6-Dichloro-2-bromo-3-formyl-1-(5-O-acetyl-β-D-ribofuranosyl)indole
C[O-].[Na+]
sodium methoxide
CO.O
MeOH H2O
O=Cc1c(Br)n([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c2cc(Cl)c(Cl)cc12
4.137
المردود 47.0%
O=Cc1c(Br)n([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c2cc(Cl)c(Cl)cc12
5,6-Dichloro-2-bromo-3-formyl-1-(β-D-ribofuranosyl)indole
المردود 47.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىwas consumed (TLC)
  2. 2
    workup.ADDITIONWater (30 mL) was added
  3. 3
    أخرىthe solution evaporated until the MeOH
  4. 4
    أخرىwas completely removed
  5. 5
    استخلاصThe residual aqueous suspension was extracted with EtOAc (3×30 mL)
  6. 6
    غسيلthe combined organic extracts washed with brine (20 mL)
  7. 7
    تجفيفdried over MgSO4
  8. 8
    ترشيحfiltered
  9. 9
    أخرىevaporated
  10. 10
    أخرىto yield a white solid
  11. 11
    workup.ADDITIONFractions containing product
  12. 12
    أخرىevaporated
  13. 13
    أخرىto yield a white solid which
  14. 14
    أخرىwas recrystallized from MeOH and H2O

الإجراء التجريبي

5,6-Dichloro-2-bromo-3-formyl-1-(5-O-acetyl-β-D-ribofuranosyl)indole (4.136, 101 mg, 0.22 mmol) was dissolved in dry MeOH (10 mL) to which was added sodium methoxide (25 mg, 0.46 mmol). The solution was stirred at room temperature for 15 min, until the starting material was consumed (TLC). Water (30 mL) was added and the solution evaporated until the MeOH was completely removed. The residual aqueous suspension was extracted with EtOAc (3×30 mL) and the combined organic extracts washed with brine (20 mL), dried over MgSO4, filtered and evaporated to yield a white solid. The solid was dissolved in MeOH (1 mL) and subjected to column chromatography (40×350 mm) on C18-reverse phase silica gel with 75% MeOH/H2O. Fractions containing product were pooled and evaporated to yield a white solid which was recrystallized from MeOH and H2O to yield 43 mg (47%) of 4.137 as a pale tan powder: mp 210-211° C.; Rf0.2 (10% MeOH/CHCl3); 1H-NMR (500 MHz, DMSO-d6): δ 9.95 (s, 1H), 8.69 (s, 1H), 8.28 (s, 1H), 6.06 (d, 1H), 5.49-5.43 (m, 2H, D2O exch.), 5.31 (d, 1H, D2O exch.), 4.44 (q, 1H), 4.18 (m, 1H), 4.04 (d, 1H), 3.77-3.71 (m, 2H). 13C-NMR (125 MHz, DMSO-d6): δ 185.53, 134.05, 128.85, 126.58, 126.47, 125.31, 120.56, 116.00, 114.68, 90.27, 86.55, 71.69, 69.62, 60.98. HRMS (EI) m/z calcd. for C14H12BrCl2NO5 422.9276, found 422.9271. Anal calcd for C14H12BrCl2NO5: C, 39.56; H, 2.85; N, 3.30. Found: C, 39.77; H, 3.03; N, 3.32.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07625871B2uspto-grants-2009_12