2-benzyloxycarbonylamino-3-[1-(2-trimethylsilanyl-ethanesulfonyl)-1H-indol-5-yl]-acrylic acid methyl ester → (+/-)-2-Amino-3-[1-(2-trimethylsilanyl-ethanesulfonyl)-1H-indol-5-yl]-propionic Acid Methyl Ester

HRID 1353509Notes

Reaction equation

HRID 1353509 reaction equation
[CH3:1][O:2][C:3](=[O:35])[C:4]([NH:24]C(OCC1C=CC=CC=1)=O)=[CH:5][C:6]1[CH:7]=[C:8]2[C:12](=[CH:13][CH:14]=1)[N:11]([S:15]([CH2:18][CH2:19][Si:20]([CH3:23])([CH3:22])[CH3:21])(=[O:17])=[O:16])[CH:10]=[CH:9]2>[Pd].CO>[CH3:1][O:2][C:3](=[O:35])[CH:4]([NH2:24])[CH2:5][C:6]1[CH:7]=[C:8]2[C:12](=[CH:13][CH:14]=1)[N:11]([S:15]([CH2:18][CH2:19][Si:20]([CH3:23])([CH3:22])[CH3:21])(=[O:17])=[O:16])[CH:10]=[CH:9]2

Participants

4

Reactant 1

HCID 684643132-benzyloxycarbonylamino-3-[1-(2-trimethylsilanyl-ethanesulfonyl)-1H-indol-5-yl]-acrylic acid methyl ester

Product 1

HCID 68707458(+/-)-2-Amino-3-[1-(2-trimethylsilanyl-ethanesulfonyl)-1H-indol-5-yl]-propionic Acid Methyl EsterYield 76.1%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 887MethanolSolvent

Procedure

To a flame dried 500 mL of round bottom flask was added 2-benzyloxycarbonylamino-3-[1-(2-trimethylsilanyl-ethanesulfonyl)-1H-indol-5-yl]-acrylic acid methyl ester (2.24 h, 4.36 mmol), methanol (100 mL) and 10% palladium on charcoal (0.52 g). The mixture was degassed and purged with hydrogen five times. It was stirred at room temperature for 1 h and filtered through a pad of celite. Solvents were removed and the residue was subjected to flash chromatography using ethyl acetate/hexanes (1:1 and 2:1) containing 1% triethylamine to afford the tile compound as a colorless viscous liquid (1.27 g, 76%), which solidified upon cooling.

Workup

  1. customTo a flame dried 500 mL of round bottom flask
  2. customThe mixture was degassed
  3. custompurged with hydrogen five times
  4. filtrationfiltered through a pad of celite
  5. customSolvents were removed
  6. additioncontaining 1% triethylamine

Sources & evidence

ORD record
ord-0195e952011d4fe48e373e51c988f3c5
Source dataset
uspto-grants-2007_05
Patent number
US07220862B2

Reaction notes

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