反应详情
EQUATION
反应方程式
REACTANTS
反应物
N,N-Dimethylformamide
C3H7NO
Dichloromethane
CH2Cl2
Diisopropylethylamine
C8H19N
2 次
Di-tert-butyl dicarbonate
C10H18O5
Tri(dimethylamino)benzotriazol-1-yloxyphosphonium hexafluorophosphate
C12H22F6N6OP2
4-Phenyl-1,2,3,6-tetrahydropyridine hydrochloride
C11H14ClN
未命名化合物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A mixture of (2S,3S,5R)-5-hydroxy-3-(methoxycarbonyl)piperidine-2-carboxylic acid (1.851 g, 0.009110 mol), 4-phenyl-1,2,3,6-tetrahydropyridine hydrochloride (2.14 g, 0.0109 mol) and benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (4.83 g, 0.0109 mol) in N,N-dimethylformamide (15.0 mL, 0.194 mol) was stirred at rt for 5 min, then treated with N,N-diisopropylethylamine (3.81 mL, 0.0219 mol) at rt for 2 h. The reaction mixture was diluted with methylene chloride (10.0 mL, 0.156 mol). The resultant mixture was then treated with N,N-diisopropylethylamine (3.17 mL, 0.0182 mol), followed by di-tert-butyldicarbonate (3.98 g, 0.0182 mol) at rt overnight. The reaction was diluted with water, extracted with EtOAc. The combined orgnica layers were washed with brine, dried, and concentrated to dry in vacuo. The residue was applied on silica gel, eluting with 0 to 80% EtOAc in hexane, to give The titled compound (2.10 g, 51.9%). MS (ESI): (M+H-Boc)+=345.1.
WORKUP
后处理
- extractionextracted with EtOAc
- washThe combined orgnica layers were washed with brine
- customdried
- concentrationconcentrated
- customto dry in vacuo
- washeluting with 0 to 80% EtOAc in hexane