反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a solution (R)-tert-butyl 2-(6-(1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)hexylthio)ethyl(2-hydroxy-2-(4-hydroxy-2-oxo-2,3-dihydrobenzo[d]thiazol-7-yl)ethyl)carbamate (example 101, step g) (0.093 g) in DMF (3 mL) was added triethylamine (0.062 mL) and 2-isopropyl-thiazole-4-carboxylic acid (0.025 g) followed by O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (0.079 g). The resultant mixture was stirred at RT for 4 h then 4 drops of ‘880’ aqueous ammonia were added and the mixture was stirred for 15 min. Brine and ethyl acetate were added to the solution and the phases were separated, then the organic phase was extracted with ethyl acetate (×2). The combined organic phase was dried over sodium sulphate, filtered and evaporated in vacuo. The residue was dissolved in DCM (2 mL) then trifluoroacetic acid (1 mL) was added. The solution was left to stand at RT for 40 min then toluene (20 mL) was added and the mixture was concentrated in vacuo. A further amount of toluene was added and the mixture concentrated again before the material was azeotroped with acetonitrile. Purification was by preparative HPLC (Phenomenex Gemini®, Gradient: 10-40% acetonitrile in 0.1% aqueous formic acid). The fractions containing product were combined and freeze dried to give the titled compound as a colourless solid. Yield 0.016 g.
WORKUP
后处理
- customthe phases were separated
- extractionthe organic phase was extracted with ethyl acetate (×2)
- dry with materialThe combined organic phase was dried over sodium sulphate
- filtrationfiltered
- customevaporated in vacuo
- dissolutionThe residue was dissolved in DCM (2 mL)
- additiontrifluoroacetic acid (1 mL) was added
- waitThe solution was left
- waitto stand at RT for 40 min
- additiontoluene (20 mL) was added
- concentrationthe mixture was concentrated in vacuo
- additionA further amount of toluene was added
- concentrationthe mixture concentrated again before the material
- customwas azeotroped with acetonitrile
- customPurification
- additionThe fractions containing product
- customfreeze dried