HRID501678

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：C=CC[C@@H](C(=O)OC)N(C)C(=O)c1sccc1OCC

HCID68466211

未命名化合物

结构：C=CCC[C@@H](C(=O)OC)N(C)S(=O)(=O)CCC(F)(F)F

HCID86622317

未命名化合物

PRODUCTS

生成物

结构：C=CC[C@@H](C(=O)O)N(C)C(=O)c1sccc1OCC

HCID59423696

未命名化合物

收率 89%

PROCEDURE

实验过程

Step N (2): Same procedure as Step A (3). (S)-Methyl 2-(3,3,3-trifluoro-N-methylpropylsulfonamido)hex-5-enoate from Step N (1) was subjected to the ester hydrolysis protocol. The procedure provided 68 mg (89% yield) of the title compound as a colorless oil. LC-MS (M+H)+=284.27.