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HRID2418082

反应详情

EQUATION

反应方程式

HRID 2418082 的结构方程式

REACTANTS

反应物

4
结构：CN(C)Cc1ccc(CSCCN)o1
HCID162203

5-((2-Aminoethyl)thiomethyl)-N,N-dimethyl-2-furanmethanamine

C10H18N2OS

结构：COC1=NS(=O)(=O)N=C1OC
HCID12230538

3,4-dimethoxy-1,2,5-thiadiazole 1,1-dioxide

C4H6N2O4S

结构：NCCSCc1ccsn1
HCID12951537

2-{[(1,2-Thiazol-3-yl)methyl]sulfanyl}ethan-1-amine

C6H10N2S2

结构：COC1=NS(=O)(=O)N=C1NCCSCc1ccc(CN(C)C)o1
HCID178494329

未命名化合物

PRODUCTS

生成物

1
结构：CN(C)Cc1ccc(CSCCNC2=NS(=O)(=O)N=C2NCCSCc2ccsn2)o1
HCID178483227

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

1
结构：CO
溶剂HCID887

Methanol

CH4O

PROCEDURE

实验过程

When a methanol suspension of 3,4-dimethoxy-1,2,5-thiadiazole 1,1-dioxide is reacted with one equivalent of 2-[(5-dimethylaminomethyl-2-furyl)methylthio]ethylamine according to the procedure described in Example 17, Step A, and the resultant 3-{2-[(5-dimethylaminomethyl-2-furyl)methylthio]ethylamino}-4-methoxy-1,2,5-thiadiazole 1,1-dioxide is treated with one equivalent of 2-[3-isothiazolylmethylthio]ethylamine, the title compound is produced.