HRID2389127

反应详情

EQUATION

反应方程式

HRID 2389127 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Zinc (0.194 g, 2.96 mmol) was added to a solution of 4-[6-(trans-4-tert-butyl-cyclohexyloxy)-5-trifluoromethyl-naphthalen-2-yl]-4-nitro-butyric acid (0.102 g, 0.212 mmol) in acetic acid (3.00 mL, 52.8 mmol). The mixture was stirred for 2 hours at room temperature. HPLC analysis showed that the reaction was complete. The mixture was filtered and the filtrate was concentrated to dryness under reduced pressure. The resulting crude product was dissolved in DMSO (4 mL) and purified by HPLC. The product was dried for 2 days under vacuum to give 28 mg of the title compound as a white solid (26% yield). MS: m/z=435.66 [M-16]+. 1H NMR (MeOD, 400 MHz): δ=8.24-8.30 (m, 1 H), 8.09-8.14 (m, 1 H), 7.92-7.96 (m, 1 H), 7.56-7.65 (m, 2 H), 4.45-4.57 (m, 2 H), 2.65-2.69 (m, 2 H), 2.26-2.46 (m, 4 H), 2.18-2.26 (m, 2 H), 1.87-1.97 (m, 2 H), 1.45-1.58 (m, 2 H), 1.18-1.31 (m, 2 H), 1.06-1.17 (m, 1 H), 0.92 (s, 9 H)

WORKUP

后处理

  1. filtrationThe mixture was filtered
  2. concentrationthe filtrate was concentrated to dryness under reduced pressure
  3. dissolutionThe resulting crude product was dissolved in DMSO (4 mL)
  4. custompurified by HPLC
  5. customThe product was dried for 2 days under vacuum