HRID1971257

反应详情

EQUATION

反应方程式

HRID 1971257 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

6

CONDITIONS

反应条件

温度
120 °C

PROCEDURE

实验过程

In a ½ dram vial, 5-chloro-imidazo[1,2-a]pyrimidine (20.2 mg, 0.13 mmol), Zn(CN)2 (9.3 mg, 0.079 mmol), Pd2(dba)3 (3.0 mg, 0.003 mmol) and DPPF (3.6 mg, 0.006 mmol) are treated with DMF (300 μL) and H2O (3 μl). The vial is flushed and then sealed under argon and heated to 120° C. overnight. At RT, the vial is treated with NaOH (1M, 0.5 mL) and i-PrOAc (0.5 mL), and the upper organic layer is purified via strong cation exchange chromatography. The base-eluted solution is concentrated to dryness and treated with HCl (conc., 0.1 mL) and shaken at RT for 1 h and then at 100° C. for an additional 1 h. The reaction is concentrated to dryness under a stream of nitrogen and treated with adamantan-1-yl-methylamine hydrochloride (8.1 mg, 0.040 mmol), TEA (10% (v/v) ACN, 200 μL), and 2-chloro-1,3-dimethyl-4,5-dihydro-3H-imidazolium chloride (0.2 M ACN, 200 μL, 0.040 mmol). The reaction is sealed under nitrogen and shaken at RT for 1 h. NaOH (1M, 0.5 mL) and i-PrOAc (0.5 mL) are added, and the upper organic layer is removed and concentrated to dryness. The residue is purified via silica gel chromatography using EtOAc followed by TEA/MeOH/EtOAc (2.5:2.5:95% v/v/v) to afford the title compound. NMR (400 MHz, CDCl3) δ 1.59 (m, 6H), 1.64 (m, 3H), 1.72 (m, 3H), 1.99 (m, 3H), 3.18 (d, J=6.4, 2H), 7.68 (d, J=1.2, 1H), 7.83 (d, J=6.8, 1H), 7.99 (d, J=1.6, 1H), 8.12 (bs, 1H), 8.58 (d, J=6.8, 1H).

WORKUP

后处理

  1. customThe vial is flushed
  2. customsealed under argon
  3. additionAt RT, the vial is treated with NaOH (1M, 0.5 mL) and i-PrOAc (0.5 mL)
  4. customthe upper organic layer is purified via strong cation exchange chromatography
  5. concentrationThe base-eluted solution is concentrated to dryness
  6. additiontreated with HCl (conc., 0.1 mL)
  7. waitat 100° C. for an additional 1 h
  8. concentrationThe reaction is concentrated to dryness under a stream of nitrogen
  9. customThe reaction is sealed under nitrogen
  10. stirringshaken at RT for 1 h
  11. customthe upper organic layer is removed
  12. concentrationconcentrated to dryness
  13. customThe residue is purified via silica gel chromatography