HRID1805388

反应详情

EQUATION

反应方程式

HRID 1805388 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

(1S,2R) and (1R,2S)-2-(4-chlorophenyl)-1′-(1-trityl-1H-imidazol-4-yl)spiro [cyclopropane-1,3′-indolin]-2′-one (115 mg, 0.2 mmol) was dissolved in DCM (2 mL) and water (0.5 mL). TFA (0.1 mL) was added dropwise at 0° C. The mixture was stirred for 14 hours at room temperature. The mixture was poured into the sat. NaHCO3, extracted with DCM (3×10 mL), dried and concentrated to give the title product. The residue was dissolved in 2 mL of DMF. Purification by preparative HPLC to give the title compound as white powder (60 mg, 89%). 1H NMR (400 MHz, DMSO-d6) δppm 2.13 (dd, J=9.09, 5.05 Hz, 1 H) 2.42 (dd, J=8.08, 4.80 Hz, 1 H) 3.23 (t, J=8.72 Hz, 1 H) 6.20 (d, J=7.58 Hz, 1 H) 6.81 (t, J=7.20 Hz, 1 H) 7.16 (t, J=7.83 Hz, 1 H) 7.30-7.45 (m, 5H) 7.66 (s, 1 H) 8.27 (s, 1 H). LC/MS m/e calcd. for C19H14ClN3O 335, observed (M+H)+: 336.3.

WORKUP

后处理

  1. extractionextracted with DCM (3×10 mL)
  2. customdried
  3. concentrationconcentrated