HRID2177970
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
PROCEDURE
实验过程
A mixture of 1-(1-methyl-1H-pyrazol-3-yl)-2-(thiophen-3-yl)ethanone (Intermediate 58) (750 mg, 3.6 mmol), 4-hydroxy-3-methoxy-5-nitrobenzaldehyde (782 mg, 3.7 mmol), urea (666 mg, 11.1 mmol) and conc. HCl (0.2 mL) in EtOH (10 mL) was refluxed overnight. The mixture was concentrated under reduced pressure to dryness and purified by prep-HPLC (0.1% TFA as additive) to give Compound 119 (1.3 g, yield 81%). 1H NMR and MS (ESI) characterization included for the individual enantiomers, see Compound 149 and Compound 150.
WORKUP
后处理
- temperaturewas refluxed overnight
- concentrationThe mixture was concentrated under reduced pressure to dryness
- custompurified by prep-HPLC (0.1% TFA as additive)