Acetic Acid → HCID 22871973, compound

HRID 1938910Notes

Reaction equation

HRID 1938910 reaction equation
[CH3:1][N:2]1[C:19](=[O:20])[CH2:18][CH2:17][C@@:16]2([CH3:21])[C@H:3]1[CH2:4][CH2:5][C@@H:6]1[C@@H:15]2[CH2:14][CH2:13][C@@:11]2([CH3:12])[C@H:7]1[CH2:8][CH2:9][CH:10]2[CH:22]=[N:23]O.C(O)C.C(O)(=O)C.[H][H]>O=[Pt]=O.O>[NH2:23][CH2:22][CH:10]1[CH2:9][CH2:8][C@H:7]2[C@H:6]3[C@H:15]([CH2:14][CH2:13][C@:11]12[CH3:12])[C@:16]1([CH3:21])[C@H:3]([N:2]([CH3:1])[C:19](=[O:20])[CH2:18][CH2:17]1)[CH2:4][CH2:5]3

Participants

7

Procedure

A mixture of (38) (0.67 g, 2.0 mM), ethanol (100 mL), glacial acetic acid (8 mL) and water (4 mL) was reduced in a hydrogen atmosphere (40 p.s.i.) at room temperature in the presence of PtO2 until TLC analysis indicated complete reduction. The filtered reaction mixture was concentrated in vacuo, the residue taken up in chloroform, and the chloroform solution washed with fresh dilute sodium hydrogen carbonate solution and dried (Na2SO4). Concentration of the filtered chloroform solution followed by trituration of the residue obtained with hexane containing a small amount of ether yielded (39) as an off-white solid.

Workup

  1. customThe filtered reaction mixture
  2. concentrationwas concentrated in vacuo
  3. washthe chloroform solution washed with fresh dilute sodium hydrogen carbonate solution
  4. dry with materialdried (Na2SO4)
  5. customobtained with hexane containing a small amount of ether

Sources & evidence

ORD record
ord-9a955527fc4a4d849961555ff33d91fb
Source dataset
uspto-grants-1997_12
Patent number
US05693809

Reaction notes

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