反应详情
EQUATION
反应方程式
REACTANTS
反应物
4-Methylmorpholine
C5H11NO
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide
C8H17N3
2-Propanol, 1,3-diamino-
C3H10N2O
Leucine, N-carboxy-, N-benzyl ester, L-
C14H19NO4
1-Hydroxybenzotriazole
C6H5N3O
4-(3-Chloro-2-Cyanophenoxy)Benzene-1-Sulfonyl Chloride
C13H7Cl2NO3S
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
Cbz-leucine (660 mg, 2.5 mmol), EDCI (480 mg, 2.5 mmol), HOBT (340 mg, 2.5 mmol) was dissolved in DMF (10 ml) with 1,3-diamino-propan-2-ol (225 mg, 2.5 mmol) and was stirred at RT overnight. N-methyl morpholine (0.41 ml, 3.75 mmol) was added followed by 4-(3-Chloro-2-cyano-phenoxy)-phenyl sulfonyl chloride (820 mg, 2.5 mmol, Maybridge) was added and the reaction was stirred 3 h at RT. The reaction was partitioned between water and EtOAc and the combined organics were dried with magnesium sulfate, then concentrated in vacuo. The crude 1-(Cbz-leucinyl)-amino-3-(4-(3-chloro-2-cyano-phenoxy)-phenyl sulfonamido)-propan-2-ol was then dissolved in acetone (5.0 ml) and Jones reagent (3.0 ml, 1.5 M) was added dropwise, and the reaction was stirred overnight at RT. The excess Jones reagent was then quenched with isopropanol (1.0 ml), then the reaction was diluted with EtOAc (20 ml) and was extracted with water (2×20 ml) to remove the inorganic salts. The combined organics were dried with magnesium sulfate, filtered, concentrated, and chromatographed (silica gel, 2-5% MeOH/methylene chloride), then the product was triturated from methylene chloride to give the title compound as a white solid (26 mg, 2%). MS(ES) M+H+=627.
WORKUP
后处理
- additionwas added
- stirringthe reaction was stirred 3 h at RT
- customThe reaction was partitioned between water and EtOAc
- dry with materialthe combined organics were dried with magnesium sulfate
- concentrationconcentrated in vacuo
- dissolutionThe crude 1-(Cbz-leucinyl)-amino-3-(4-(3-chloro-2-cyano-phenoxy)-phenyl sulfonamido)-propan-2-ol was then dissolved in acetone (5.0 ml)
- additionJones reagent (3.0 ml, 1.5 M) was added dropwise
- stirringthe reaction was stirred overnight at RT
- customThe excess Jones reagent was then quenched with isopropanol (1.0 ml)
- additionthe reaction was diluted with EtOAc (20 ml)
- extractionwas extracted with water (2×20 ml)
- customto remove the inorganic salts
- dry with materialThe combined organics were dried with magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customchromatographed (silica gel, 2-5% MeOH/methylene chloride)
- customthe product was triturated from methylene chloride