HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1200243Generated: October 30, 2026
2-(Dimethylaminomethyl)-4-(2-aminoethylthiomethyl)thiazole → HCID 136486310, compound
https://huagongshe.com/reaction/1200243
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Dimethylaminomethyl)-4-(2-aminoethylthiomethyl)thiazole | HCID 10977318 | — |
| Reactant | 1,2-Dimethyl-3-nitroisothiourea | HCID 136227017 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 136486310 | HCID 136486310 | — |
Reaction Steps
A reaction mixture was prepared containing 1.2 g. of 2-(2-dimethylaminomethyl-4-thiazolylmethylthio)ethylamine, 0.77 g. of S-methyl-N-methyl-N'-nitroisothiourea and 10 ml. of methanol. The reaction mixture was heated under reflux for 4.25 hours, after which time the solvent was removed by evaporation. The partially solid residue was chromatographed over silica using a gradient elution technique employing ethyl acetate containing increasing quantities of methanol as the eluant. Fractions shown by tlc to contain N-methyl-N'-2-(2-dimethylaminomethyl-4-thiazolylmethylthio)ethyl-N"-nitroguanidine formed in the above reaction were pooled and the solvent removed from the pooled fractions. Trituration of the resulting residue with ether yielded a crystalline solid which, upon recrystallization from a methanol-ethyl acetate solvent mixture, yielded 0.83 g. of crystals melting at about 86.5°-88° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04904792 |
|---|
| Source dataset | uspto-grants-1990_02 |
|---|
| ORD ID | ord-7a8e88ecbf984efaa013067f16f4f198 |
|---|
| Source note | uspto-grants-1990_02 |
|---|