Methylhydrazine → HCID 15747245, compound

HRID 323529Notes

Reaction equation

HRID 323529 reaction equation
[Si:1]([O:18][C@@H:19]1[C@@H:23]([CH2:24][O:25][N:26]2C(=O)C3=CC=CC=C3C2=O)[O:22][C@@H:21]([N:37]2[CH:45]=[C:43]([CH3:44])[C:41](=[O:42])[NH:40][C:38]2=[O:39])[CH2:20]1)([C:14]([CH3:17])([CH3:16])[CH3:15])([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CNN>C(Cl)Cl>[NH2:26][O:25][CH2:24][C@H:23]1[O:22][C@@H:21]([N:37]2[CH:45]=[C:43]([CH3:44])[C:41](=[O:42])[NH:40][C:38]2=[O:39])[CH2:20][C@@H:19]1[O:18][Si:1]([C:14]([CH3:17])([CH3:16])[CH3:15])([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

4

Conditions

Temperature
0 °C

Procedure

To a stirred solution of 3′-O-(t-butyldiphenylsilyl)-5′-O-phthalimidothymidine (10 g, 16 mmol) in dry CH2Cl2 (100 ml) was added methylhydrazine (1.3 ml, 24 mmol) under argon at room temperature and solution stirred for 12 h. The solution was cooled (0° C.) and filtered. The white residue was washed with CH2Cl2 (2×25 ml) and combined filtrates were evaporated to furnish gummy residue. The residue on purification by silica gel column chromatography (elution with CH2Cl2:MeOH, 98:2, v/v) furnished 7.03 g (89%) of 5′-O-amino-3′-O-(t-butyldiphenylsilyl)thymidine that crystallized from CH2Cl2/MeOH mp 141-143° C. 1H NMR (DMSO-d6) δ 11.29 (s, 1, NH), 7.42-7.62 (m, 11, TBDPhH, C6H), 6.25 (dd, 1, H1′, J1′,2′=8.4 Hz, J1′,2″=6.3 Hz), 6.02 (s, 2, NH2), 4.35 (m, 1, H4′), 4.04 (m, 1, H3′), 3.34-3.51 (m, 2, H5′, H5″), 2.04 (m, 2, H2′,2″), 1.73 (s, 3, CH3), 1.03 (s, 9, C(CH3)3). Anal. Calcd. for C26H33O5N3Si: C, 63.00; H, 6.71; N, 8.48. Found: C, 62.85; H, 6.67; N, 8.32.

Workup

  1. filtrationfiltered
  2. washThe white residue was washed with CH2Cl2 (2×25 ml)
  3. customwere evaporated
  4. customto furnish gummy residue
  5. customThe residue on purification by silica gel column chromatography (
  6. washelution with CH2Cl2

Sources & evidence

ORD record
ord-14edaa3934484578be69f33b8e60bcc9
Source dataset
uspto-grants-2001_04
Patent number
US06214551B1

Reaction notes

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