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HRID1603514

反应详情

EQUATION

反应方程式

HRID 1603514 的结构方程式

REACTANTS

反应物

2
结构：NS(=O)(=O)NCc1csc2cncn12
HCID19605164

未命名化合物

结构：C=CCOC(=O)O[C@H](C)[C@H]1C(=O)N2C(C(=O)OCC=C)=C(CO)C(C)[C@H]12
HCID131721461

未命名化合物

PRODUCTS

生成物

1
结构：CC1C(Cn2cc3scc(CNS(N)(=O)=O)[n+]3c2)=C(C(=O)[O-])N2C(=O)[C@H]([C@@H](C)O)[C@@H]12
HCID178427987

未命名化合物

收率 12.9%

PROCEDURE

实验过程

The same procedure as in Example 1 was repeated except that 88 mg of allyl (5R,6S)-6-[(1R)-1-allyloxycarbonyloxyethyl]-2-hydroxymethyl-1-methyl-1-carbapen-2-em-3-carboxylate and 87 mg of 3-(aminosulfonyl)aminomethylimidazo[5,1-b]thiazole were used, thereby obtaining 14.2 mg of the title compound.