HRID533126

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CC1(C)OB(C2=CCN(S(C)(=O)=O)CC2)OC1(C)C

HCID67973497

未命名化合物

结构：CC(C)(C)OC(=O)N1CCC([C@]2(C)Cc3cc(Cl)ncc3O2)CC1

HCID86674904

未命名化合物

PRODUCTS

生成物

结构：CC(C)(C)OC(=O)N1CCC([C@@]2(C)Cc3cc(C4=CCN(S(C)(=O)=O)CC4)ncc3O2)CC1

HCID86686881

未命名化合物

PROCEDURE

实验过程

The title compound is prepared from (S)-4-(5-chloro-2-methyl-2,3-dihydro-furo[2,3-c]pyridin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester and 1-methanesulfonyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1,2,3,6-tetrahydro-pyridine following a procedure analogous to that described for Intermediate 10. LC (method 4): tR=1.02 min; Mass spectrum (ESI+): m/z=478 [M+H]+.