Sodium Sulfate → HCID 86585350, compound

HRID 1356289Notes

Reaction equation

HRID 1356289 reaction equation
[C:1]1([CH2:7][O:8][C:9](=[O:29])[NH:10][CH2:11][CH2:12][C:13]2[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[NH:15][C:14]=2[C:22]([CH3:28])([CH3:27])[CH:23]([OH:26])CO)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CC(C)=O.C(Cl)Cl.[O-]S([O-])(=O)=O.[Na+].[Na+]>O>[C:1]1([CH2:7][O:8][C:9](=[O:29])[NH:10][CH2:11][CH2:12][C:13]2[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[NH:15][C:14]=2[C:22]([CH3:27])([CH3:28])[CH:23]=[O:26])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

5

Procedure

To a solution of (±)-N-[2-[2-(2,3-dihydroxy-1,1-dimethylpropyl)-1H-indol-3-yl]ethyl]-carbamic acid phenylmethyl ester (0.323 g, 0.81 mol) in 1:1 acetone/CH2Cl2 (19.5 mL) was added NaIO4 (0.350 g, 1.64 mmol) in H2O (2.2 mL). The reaction mixture was stirred for 3 h at rt. Solid Na2SO4 was added. The mixture was filtered. The filtrate was extracted with CH2Cl2. The CH2Cl2 extracts were dried, filtered, and concentrated to an oil. This oil was purified by silica chromatography to give the title compound: TLC Rf=0.31 (1:1 heptane/EtOAc); MS (ESI+) m/z 365.2; 1H NMR (300 MHz, CDCl3) δ 9.56 (1H), 8.11 (1H), 7.64 (1H), 7.37 (5H), 7.21 (1H), 7.13 (1H), 5.14 (2H), 4.92 (1H), 3.45 (2H), 2.95 (2H), 1.60 (6H).

Workup

  1. filtrationThe mixture was filtered
  2. extractionThe filtrate was extracted with CH2Cl2
  3. dry with materialThe CH2Cl2 extracts were dried
  4. filtrationfiltered
  5. concentrationconcentrated to an oil
  6. customThis oil was purified by silica chromatography

Sources & evidence

ORD record
ord-ee606670b13b4bbb9e6a5f1995c26f10
Source dataset
uspto-grants-2003_07
Patent number
US06586421B2

Reaction notes

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