反应详情
EQUATION
反应方程式
REACTANTS
反应物
Triethylamine
C6H15N
Acetic acid, 3-benzo(b)thienyl-
C10H8O2S
1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride
C8H18ClN3
1H-Benzotriazol-1-ol--water (1/1)
C6H7N3O2
N-[3-(6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenyl)methanesulfonamide
C13H18N2O2S
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a solution of 2-(1-benzothiophen-3-yl)acetic acid (118 mg, 0.62 mmol) in N,N-dimethylformamide (13 ml) was added 1-hydroxybenzotriazole monohydrate (100 mg, 0.66 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (170 mg, 0.88 mmol). After stirring at room temperature for 5 min the mixture was treated with the hydrochloride salt of N-[3-(6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenyl]methanesulfonamide (Preparation 53, 200 mg, 0.66 mmol) and triethylamine (133 mg, 1.32 mmol). The reaction mixture was stirred at room temperature for 72 h before concentrating in vacuo. Water (10 ml) was added and the reaction mixture was extracted with ethyl acetate (2×15 ml). The combined organic extracts were washed with water (10 ml) and saturated brine (10 ml), dried (Na2SO4), filtered and concentrated in vacuo to give a light brown oil. The residue was purified by chromatography using a Sep-Pak™ cartridge packed with silica gel (10 g) eluting with dichoromethane:ethanol:0.88 ammonia (300:8:1) to afford the title compound as a white foam (99 mg, 34%).
WORKUP
后处理
- stirringThe reaction mixture was stirred at room temperature for 72 h
- concentrationbefore concentrating in vacuo
- additionWater (10 ml) was added
- extractionthe reaction mixture was extracted with ethyl acetate (2×15 ml)
- washThe combined organic extracts were washed with water (10 ml) and saturated brine (10 ml)
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
- customto give a light brown oil
- customThe residue was purified by chromatography
- washeluting with dichoromethane