HRID362492

反应详情

EQUATION

反应方程式

HRID 362492 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

DMSO (0.06 mL, 0.9 mmol) was added to a solution of oxalyl chloride (0.14 mL, 2.0M, 0.28 mmol, in 4 mL of methylene chloride) and the solution was then stirred for 10 minutes under a nitrogen atmosphere at -78° C. A solution of N-[(1-methylindole-2-carbonyl)valinyl]-3-amino-4-hydroxy-5-fluoropentanoic acid, t-butyl ester (85 mg, 0.18 mmol) in dry methylene chloride (1 mL), was added dropwise to the reaction mixture and the mixture was stirred for 15 minutes at -78° C. Triethylamine (0.15 mL, 1.08 mmol) was added dropwise to the reaction mixture and the mixture was stirred for 10 minutes at -78° C. and then was allowed to warm to room temperature. The reaction mixture was partitioned between ethyl acetate and 5% KHSO4 solution and the aqueous layer was back-extracted with ethyl acetate. The combined ethyl acetate solutions were washed with 5% KHSO4 solution and brine, dried over sodium sulfate, and concentrated to give a brown foam. The foam was triturated with ether to afford the title product as a light brown powder (64 mg). MS for C24H31ClFN3O5 : (MH)- =494/496.

WORKUP

后处理

  1. stirringthe mixture was stirred for 15 minutes at -78° C
  2. stirringthe mixture was stirred for 10 minutes at -78° C.
  3. temperatureto warm to room temperature
  4. customThe reaction mixture was partitioned between ethyl acetate and 5% KHSO4 solution
  5. extractionthe aqueous layer was back-extracted with ethyl acetate
  6. washThe combined ethyl acetate solutions were washed with 5% KHSO4 solution and brine
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated
  9. customto give a brown foam
  10. customThe foam was triturated with ether