反应详情
EQUATION
反应方程式
REACTANTS
反应物
Dichloromethane
CH2Cl2
2 次
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide
C8H17N3
Diisopropylethylamine
C8H19N
(alpha,alpha,alpha-Trifluoro-4-tolyl)acetic acid
C9H7F3O2
1H-Benzotriazol-1-ol--water (1/1)
C6H7N3O2
(1R,2R)-N-Methyl-2-(pyrrolidin-1-yl)cyclohexan-1-amine
C11H22N2
PRODUCTS
生成物
CONDITIONS
反应条件
- 温度
- 5 °C
PROCEDURE
实验过程
To a solution of 4-trifluoromethylphenyl acetic acid (1.45 g, 7.08 mmol) in 10 mL of dry CH2Cl2 under a nitrogen atmosphere was added 1-hydroxybenzotriazole hydrate (HOBT) (0.95 g, 7.08 mmol) and stirred. The reaction mixture was cooled to 0→5° C. and added solid EDCI ([1-(3-dimethylaminopropyl)-3-ethyl-carbodiimide HCl]) (1.35 g, 7.08 mmol) and stirrat this temperature for 30 min. A solution (±) 3 (1.0 g, 5.48 mmol) in 10 mL of dry CH2Cl2 was added followed by N,N-diisopropylethylamine (Hunig's Base) (0.915 g, 7.08 mmol). The reaction mixture was stirred for 24 h while warming to the room temperature. The reaction mixture was then poured on to excess of ice-cold saturated aqueous NaHCO3 solution and stirred for 30 min. After dilution with CH2Cl2, the organic was separated, washed with saturated salt solution, and dried over anhydrous Na2SO4. Removal of solvent gave a brown oil which was chromatographed on a silica gel column [solvent system: CH2Cl2:CH3OH:28% NH4OH (99:1:2)] to give the desired product as free base. The hydrochloride salt was prepared from 1M etherial HCl and recrystallized from CH2Cl2:Et2O (1:1) to give (±) 5 g HCl as a cream colored solid, 0.68 g (30%); 213-215° C.; 1H NMR (200 MHz, CDCl3) δ1.02-1.47 (m, 4H), 1.52-2.22 (m, 8H), 2.75-2.90 (m, 2H), 2.94 (s, 3H), 3.07 (m, 1H), 3.37 (m, 1H), 3.62 (d, J=15.0 Hz, 1H), 3.77 (m, 1H), 4.17 (d, J=15.0 Hz, 1H), 4.57 (m, 1H), 7.30 (d, J=8.0 Hz, 2H), 7.38 (d, J=8.0 Hz, 2H). Anal. Calcd for C20H27F3N2O.HCl.0.25H2O: C, 58.68; H, 7.02; N, 6.84. Found: C, 58.68; H, 6.84; N, 6.69.
WORKUP
后处理
- stirringThe reaction mixture was stirred for 24 h
- temperaturewhile warming to the room temperature
- additionThe reaction mixture was then poured on to excess of ice-cold saturated aqueous NaHCO3 solution
- stirringstirred for 30 min
- customAfter dilution with CH2Cl2, the organic was separated
- washwashed with saturated salt solution
- dry with materialdried over anhydrous Na2SO4
- customRemoval of solvent
- customgave a brown oil which
- customwas chromatographed on a silica gel column [solvent system: CH2Cl2:CH3OH:28% NH4OH (99:1:2)]