HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851113Generated: October 27, 2026
Methylamine → N-[[[2-[[5-(Dimethylaminomethyl)-3-thienylmethyl]thio]ethyl]amino](methylamino)methylene]methanesulphonamide
https://huagongshe.com/reaction/851113
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 2-[(5-Dimethylaminomethyl-3-thienyl)methylthio]ethylamine | HCID 12926501 | — |
| Reactant | N-[bis(methylsulfanyl)methylidene]methanesulfonamide | HCID 13449843 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[[[2-[[5-(Dimethylaminomethyl)-3-thienylmethyl]thio]ethyl]amino](methylamino)methylene]methanesulphonamide | HCID 178485212 | — |
Reaction Steps
A mixture of 4-[[2-(amino)ethyl]thio]methyl-N,N-dimethyl-2-thiophenemethanamine (0.4 g) and S,S'-dimethyl-N- (methylsulphonyl)-dithio-carbonimidic acid (0.35 g) in ethanol (10 ml) was heated at 60° C. for 1 hour. A 33% solution of methylamine in ethanol (10 ml) was added and the mixture was stirred for 20 h. The solvent was evaporated in vacuo and the residue was purified by column chromatography on silica using methanol to give the title compound (0.5 g) as an amber gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04382929 |
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| Source dataset | uspto-grants-1983_05 |
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| ORD ID | ord-97646e3e2fd1497fba083247533837ea |
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| Source note | uspto-grants-1983_05 |
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