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 suspension of cyclopropyl{6-(3,5-dichloro-4-hydroxyphenyl)-4-[trans-4-(pyrrolidin-1-ylmethyl)cyclohexylamino]quinolin-3-yl}methanone (3.69 g, 6.85 mmol) in methanol (70 mL) was added 1M HCl in water (17 mL, 17 mmol) at 0° C. The resultant solution was concentrated to an approximate volume of 30 mL. The precipitate was washed with acetonitrile to obtain the desired product as the hydrochloride salt (3.58 g) as a yellow solid: 1H NMR (500 MHz, CD3OD) δ 9.34 (s, 1H), 8.49 (s, 1H), 8.27 (dd, J=8.8, 1.8 Hz, 1H), 7.99 (d, J=8.8 Hz, 1H), 7.74 (s, 2H), 4.51-4.47 (m, 1H), 3.73-3.69 (m, 2H), 3.18-3.09 (m, 4H), 2.84 (br s, 1H), 2.44-2.40 (br s, 2H), 2.19-1.97 (m, 7H), 1.84-1.71 (m, 2H), 1.36-1.18 (m, 6H); ESI MS m/z 538 [C30H33Cl2N3O2+H]+; HPLC>99% (AUC), tR=10.65 min.
WORKUP
后处理
- concentrationThe resultant solution was concentrated to an approximate volume of 30 mL
- washThe precipitate was washed with acetonitrile