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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236257Generated: October 26, 2026

5-(Dimethylamino)methyl-2-mercaptomethyl-4-methylthiophene → N-{2-[[5-(dimethylamino)methyl-4-methyl-2-thienyl]methylthio]ethyl}-N'-(beta-hydroxyphenethyl)-2-nitro-1,1-ethenediamine

https://huagongshe.com/reaction/236257

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(Dimethylamino)methyl-2-mercaptomethyl-4-methylthiopheneHCID 13825272—
ReactantSodium methanolate methanolHCID 23694274—
ReactantN-(2-chloroethyl)-N'-(beta-hydroxyphenethyl)-2-nitro-1,1-ethenediamineHCID 67897400—
SolventMethanolHCID 887—
ProductN-{2-[[5-(dimethylamino)methyl-4-methyl-2-thienyl]methylthio]ethyl}-N'-(beta-hydroxyphenethyl)-2-nitro-1,1-ethenediamineHCID 7035701711%

Reaction Steps

In 5 ml of methanol was dissolved 0.14 g of 5-(dimethylamino)methyl-2-mercaptomethyl-4-methylthiophene, and 0.2 ml of a 3.57N sodium methoxide-methanol solution was added at room temperature in a nitrogen atomsphere, after which 0.2 g of N-(2-chloroethyl)-N'-(β-hydroxyphenethyl)-2-nitro-1,1-ethenediamine was added at one time, after which the reaction mixture was allowed to stand at room temperature for 24 hours, and the deposited substance was removed by filtration, after which the solvent was removed by distillation under reduced pressure. Chloroform was added to the resulting residue, and the insolubles were removed by filtration, after which the solvent was removed by distillation under reduced pressure, and the residue thus obtained was purified by a column chromatography (basic alumina, eluent; chloroform:methanol=10:1 by volume) to obtain 0.033 g (yield 11%) of N-{2-[[5-(dimethylamino)methyl-4-methyl-2-thienyl]methylthio]ethyl}-N'-(β-hydroxyphenethyl)-2-nitro-1,1-ethenediamine having a melting point of 114°-115° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04643849
Source datasetuspto-grants-1987_02
ORD IDord-550953e024b94c989a808e1f88eee096
Source noteuspto-grants-1987_02