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HRID723804

反应详情

EQUATION

反应方程式

HRID 723804 的结构方程式

REACTANTS

反应物

2
结构：COCCS(=O)(=O)Cl
HCID13480221

2-Methoxyethane-1-sulfonyl chloride

C3H7ClO3S

结构：Cl.O=C1O[C@@H](Cn2ccnn2)CN1c1ccc(C2=CCNCC2)c(F)c1
HCID69364214

未命名化合物

PRODUCTS

生成物

1
结构：COCCS(=O)(=O)N1CC=C(c2ccc(N3C[C@H](Cn4ccnn4)OC3=O)cc2F)CC1
HCID69363416

未命名化合物

PROCEDURE

实验过程

(5R)-3-(4-(1,2,5,6-Tetrahydropyridin-4-yl)-3-fluorophenyl)-5-(1,2,3-triazol-1-ylmethyl)-oxazolidin-2-one hydrochloride (380 mg, 1 mM) was treated with 2-methoxyethylsulfonyl chloride essentially as in Example 79. Chromatography gave the desired product (65 mg).