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
N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (36 mg, 0.19 mmol) was added to a suspension of 5-chloropicolinic acid (27 mg, 0.17 mmol) in DCM (0.5 mL). The obtained orange solution was stirred for 5 min and then added dropwise over 2 min to an ice-cooled solution of 4,4-difluoro-5″-methyl-3′H-dispiro[cyclohexane-1,2′-indene-1′,2″-imidazole]-4″,6′-diamine (Example 28d Step 1, 46 mg, 0.14 mmol) and 2 M aq. HCl (0.072 nit, 0.14 mmol) in DMF (0.5 mL). The mixture was stirred at 0° C. for 10 min and was then allowed to reach r.t. overnight. The solvent was evaporated. The crude was purified using preparative chromatography to give the title compound (11 mg, 17% yield): 1H NMR (500 MHz, DMSO-d6) δ ppm 1.23 (d, 1H), 1.51 (d, 2H), 1.66-1.98 (m, 5H), 2.18 (s, 3H), 2.99 (d, 1H), 3.08 (d, 1H), 6.63 (br. s., 1H), 7.23-7.29 (m, 2H), 7.62 (d, 1H), 8.10 (d, 1H), 8.18 (dd, 1H), 8.74 (s, 1H), 10.50 (s, 1H); MS (APCI+) m/z 458.1 [M+H]+.
WORKUP
后处理
- stirringThe mixture was stirred at 0° C. for 10 min
- waitto reach r.t. overnight
- customThe solvent was evaporated
- customThe crude was purified