HCID 69621549, compound → HCID 69621483, compound

HRID 1830974Notes

Reaction equation

HRID 1830974 reaction equation
C([O:8][C:9]1[C:33]([O:34][CH3:35])=[CH:32][C:12]2[C:13](=[O:31])[N:14]3[CH2:30][CH2:29][CH2:28][C@H:15]3[C@H:16]([OH:27])[N:17]([C:18]([O:20][CH2:21][CH2:22][Si:23]([CH3:26])([CH3:25])[CH3:24])=[O:19])[C:11]=2[C:10]=1[O:36][CH3:37])C1C=CC=CC=1>[Pd].CCO>[OH:8][C:9]1[C:33]([O:34][CH3:35])=[CH:32][C:12]2[C:13](=[O:31])[N:14]3[CH2:30][CH2:29][CH2:28][C@H:15]3[C@H:16]([OH:27])[N:17]([C:18]([O:20][CH2:21][CH2:22][Si:23]([CH3:26])([CH3:24])[CH3:25])=[O:19])[C:11]=2[C:10]=1[O:36][CH3:37]

Participants

4

Procedure

10% Pd/C catalyst (0.22 g) was added to a solution of the substrate 128 (0.95 g, 2.1 mmol) in absolute EtOH (200 mL). The reaction mixture was hydrogenated under pressure using a Parr hydrogenator at 55 psi H2 for 18 h. The reaction mixture was filtered through celite, and the celite washed with hot EtOH, taking care not to allow the filtration pad to dry out. Removal of excess solvent afforded the product as a colourless glass (0.84 g, 1.9 mmol, 92%); 1H NMR (270 MHz, CDCl3) δ0.07 (s, 9H), 0.91-0.97 (m, 2H), 2.07-2.20 (m, 4H), 3.52-3.75 (m, 2H), 3.98-4.26 (m, 9H), 5.65 (d, 1H, J=9.71 Hz), 6.26 (br s, 1H), 7.14 (s, 1H); 13C NMR (CDCl3) δ167.0, 157.3, 146.8, 143.4, 141.3, 124.9, 123.5, 105.5, 105.2, 85.8, 64.8, 64.6, 64.5, 61.2, 60.0, 56.4, 46.4, 28.9, 28.7, 23.1, 23.0, 17.3, −1.3, −1.5, −1.7.

Workup

  1. customfor 18 h
  2. filtrationThe reaction mixture was filtered through celite
  3. washthe celite washed with hot EtOH
  4. customto dry out
  5. customRemoval of excess solvent

Sources & evidence

ORD record
ord-e120d566e2c64ebd85b99ee894e571ce
Source dataset
uspto-grants-2006_06
Patent number
US07067511B2

Reaction notes

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