HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379834Generated: October 31, 2026
Dimethyl N-cyanodithioiminocarbonate → HCID 178503902, compound
https://huagongshe.com/reaction/2379834
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl N-cyanodithioiminocarbonate | HCID 66289 | — |
| Reactant | 4-(6-Aminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole | HCID 10399768 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178503902 | HCID 178503902 | — |
Reaction Steps
A mixture of 4-(6-aminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole (0.50 g) and dimethyl N-cyanodithioiminocarbonate [(CH3S)2C=N-CN] (0.29 g) in ethanol (10 ml) was refluxed for one hour to give 2-(diaminomethyleneamino)-4-[6-(3-cyano-2-methylisothioureido)methylpyridin-2-yl]thiazole of a crude product. After being concentrated to dry the above product, 40 weight % methanolic methylamine (1.6 ml) and N,N-dimethylformamide (10 ml) was added and the mixture was stirred at 60° C. for 5 hours. The solvent was evaporated in vacuo and the residue was mixed with water. The resulting precipitate was collected by filtration and recrystallized from aqueous N,N-dimethylformamide to give 4-[6-(2-cyano-3-methylguanidino)methylpyridin-2-yl]-2-(diaminomethyleneamino)thiazole (0.42 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05364871 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-b432c1196c634a4183b8dadd5cb8ec5f |
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| Source note | uspto-grants-1994_11 |
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