HRID1849989

反应详情

EQUATION

反应方程式

HRID 1849989 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

N-(tert-Butoxycarbonyl)-2,6-dimethyl-L-tyrosyl-N-{(2R)-2-[(benzyloxycarbonyl)amino]-3-phenylpropyl}-D-alaninamide (314 mg, 0.46 mmol) was dissolved in 5 mL of tetrahydrofuran and degassed by bubbling through argon gas for a few minutes. Palladium on charcoal (10% w/w, 5 mg) was added and the suspension stirred for 16 h at room temperature under 1 atmosphere of hydrogen pressure. The mixture was filtered through a short pad of celite, washed with 5 mL of tetrahydrofuran and evaporated under reduced pressure. The resulting residue was purified by column chromatography using 5% methanol in dichloromethane as eluant to provide the title compound as a clear oil (203 mg, 82%).

WORKUP

后处理

  1. customdegassed
  2. customby bubbling through argon gas for a few minutes
  3. additionPalladium on charcoal (10% w/w, 5 mg) was added
  4. filtrationThe mixture was filtered through a short pad of celite
  5. washwashed with 5 mL of tetrahydrofuran
  6. customevaporated under reduced pressure
  7. customThe resulting residue was purified by column chromatography