HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl amino guanidine hydrochloride → HCID 178485183, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl amino guanidine hydrochloride | HCID 21432264 | — |
| Reactant | Ethyl 1-methyl-5-nitro-1H-imidazole-2-carboximidate | HCID 21432269 | — |
| Reactant | HCID 178418668 | HCID 178418668 | — |
| Reactant | HCID 178479530 | HCID 178479530 | — |
| Reactant | HCID 178485182 | HCID 178485182 | — |
| Product | HCID 178485183 | HCID 178485183 | — |
| Product | HCID 178486238 | HCID 178486238 | — |
Reaction Steps
Similarly, 2-(1-methyl-5-nitro-2-imidazolecarboximidoyl)-1-amidino-1-methylhydrazine hydrochloride (IIIC) and 2-(1-methyl-5-nitro-2-imidazolecarboximidoyl)-1-methylamidinohydrazine hydrochloride (IIID) are prepared by reacting ethyl-1-methyl-5-nitro-2-imidazolecarboximidate with 1-amino-1-methylguanidine hydrochloride and 1-amino-3-methylguanidine hydrochloride, respectively. In the like manner, 2-[1-(2-hydroxyethyl)-5-nitro-2-imidazolecarboximidoyl]-1-amidinohydrazine hydrochloride (IIIE) is prepared by reacting aminoguanidine hydrochloride with the cyclic imino ester described in Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04026903 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-22eba8d554854876a952ad1f2627c3bc |
| Source note | uspto-grants-1977_05 |