HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491845Generated: October 30, 2026
Dimethyl N-cyanodithioiminocarbonate → HCID 178503905, compound
https://huagongshe.com/reaction/1491845
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl N-cyanodithioiminocarbonate | HCID 66289 | — |
| Reactant | HCID 18953880 | HCID 18953880 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178503905 | HCID 178503905 | — |
Reaction Steps
A mixture of 4-(2-aminomethylthiazol-5-yl)-2-(diaminomethyleneamino)thiazole (0.45 g) and dimethyl N-cyanodithioiminocarbonate [(CH3S)2C=N--CN] (0.26 g) in ethanol (10 ml) was refluxed for 5 hours with stirring to give 4-[2-(3-cyano-2-methylisothioureido)methylthiazol-5-yl]-2-(diaminomethyleneamino)thiazole as a crude product. After cooling to ambient temperature, 40% aqueous methylamine by weight (1.4 ml) was added to the suspension and the mixture was stirred for 12 hours at ambient temperature, The solvent was evaporated in vacuo and the residue was mixed with water (5 ml) and ethyl acetate (5 ml). The resulting precipitate was collected and recrystallized from aqueous N,N-dimethylformamide to give 4-[2-(2-cyano-3-methylguanidino)methylthiazol-5-yl]-2-(diaminomethyleneamino)thiazole (0.35 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05371097 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-233d657d550d4461b7c3843b0b3f0a8a |
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| Source note | uspto-grants-1994_12 |
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