反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 0 °C
PROCEDURE
实验过程
114.6 g of powdered 7-(3,4,5-trimetoxy-phenyl)-[1.6]naphthyridine-5-ol is suspended in 900 mL tetrahydrofurane. A solution of 115.9 g of (R)-4-[(S)-1-hydroxyethyl]-1-[(S)-1-(4-methoxyphenyl)-ethyl]-pyrrolidin-2-one and 136 g triphenylphosphine in 1000 mL tetrahydrofurane is added. The suspension is cooled to 0° C. During 40 minutes a solution of 105 mL diisopropylazodicarboxylate [DIAD] in 400 mL tetrahydrofurane is added at 0° C. to 2° C. The suspension is stirred for 3.5 hours at this temperature and then warmed up to 20° C. The solvent is evaporated under reduced pressure. The residue is suspended in 680 mL of tert-butylmethylether. Seeding crystalls of triphenylphosphinoxid are added and the mixture is stirred 16 hours at 20° C. The precipitate is filtered and and washed with tert.-butylmethylether. The fitrate is evaporated under reduced pressure. The crude product is dissolved in a mixture of 220 mL of 2-propanol and 1100 mL of isopropyl acetate at 40° C. 48 mL of trimethylchlorosilane are added during 15 minutes. The suspension is stirred for 2 hours at 20° C. The precipitate is filtered and washed with isopropyl acetate and dried at 60
WORKUP
后处理
- temperaturewarmed up to 20° C
- customThe solvent is evaporated under reduced pressure
- additionSeeding crystalls of triphenylphosphinoxid are added
- stirringthe mixture is stirred 16 hours at 20° C
- filtrationThe precipitate is filtered
- washwashed with tert.-butylmethylether
- customThe fitrate is evaporated under reduced pressure
- dissolutionThe crude product is dissolved in a mixture of 220 mL of 2-propanol and 1100 mL of isopropyl acetate at 40° C
- addition48 mL of trimethylchlorosilane are added during 15 minutes
- stirringThe suspension is stirred for 2 hours at 20° C
- filtrationThe precipitate is filtered
- washwashed with isopropyl acetate
- customdried at 60