HRID446431

反应详情

EQUATION

反应方程式

HRID 446431 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

TFA (10 mL) was cautiously added to a solution of tert-butyl 3-(2-fluoro-3-((4-(2-isopropylthiazole-4-carbonyl)-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)methyl)phenethoxy)propanoate [Example 7, step c] (3.95 g) in DCM (40 mL). The resulting mixture was stirred for 2 h. The solvent was evaporated and the residue azeotroped twice with acetonitrile. The residue was dissolved in freshly distilled 2-methyltetrahydrofuran (100 mL) and washed 3 times with a mixture of brine and saturated sodium bicarbonate solution (10:1, 100 mL). The organic phase was dried over sodium sulphate, filtered and evaporated. The residue was azeotroped 3 times with isohexane to give the subtitled compound as a white foam. Yield 2.92 g.

WORKUP

后处理

  1. customThe solvent was evaporated
  2. customthe residue azeotroped twice with acetonitrile
  3. dissolutionThe residue was dissolved in freshly distilled 2-methyltetrahydrofuran (100 mL)
  4. washwashed 3 times
  5. additionwith a mixture of brine and saturated sodium bicarbonate solution (10:1, 100 mL)
  6. dry with materialThe organic phase was dried over sodium sulphate
  7. filtrationfiltered
  8. customevaporated
  9. customThe residue was azeotroped 3 times with isohexane