反应详情
EQUATION
反应方程式
REACTANTS
反应物
Hydrochloric Acid
ClH
Triethylamine
C6H15N
1,4-Dioxane
C4H8O2
Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)
C10H15F6N6OP
tert-Butyl [(1S,2S)-2-aminocyclopentyl]carbamate
C10H20N2O2
2-(3-Methyl-1,2,4-oxadiazol-5-yl)benzoic acid
C10H8N2O3
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A mixture of 2-(3-methyl-1,2,4-oxadiazol-5-yl)benzoic acid (CAS number 475105-77-2; 0.84 g, 4.12 mmol), tert-butyl N-[(1S,2S)-2-aminocyclopentyl]carbamate (CAS number 586961-34-4; 0.75 g, 3.74 mmol), HATU (2.14 g, 5.62 mmol) and triethylamine (1.57 ml, 11.23 mmol) was stirred in dry DMF (12.5 ml) at room temperature for 17 hours. The reaction mixture was partitioned between ethyl acetate and water, washed with water and brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The crude material was then purified by column chromatography (silica, 0-100% ethyl acetate/petrol). The resulting cream solid was recrystalised from ethyl acetate, to which was then added methanol (10 ml) and HCl in 1,4-dioxane (4M, 4.68 ml, 18.72 mmol) and the reaction was stirred at room temperature for 17 hours. The reaction was concentrated in vacuo and azeotropically distilled with toluene to afford the title compound.
WORKUP
后处理
- customThe reaction mixture was partitioned between ethyl acetate and water
- washwashed with water and brine
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe crude material was then purified by column chromatography (silica, 0-100% ethyl acetate/petrol)
- customThe resulting cream solid was recrystalised from ethyl acetate, to which
- concentrationThe reaction was concentrated in vacuo
- distillationazeotropically distilled with toluene