HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-5-aminomethylthiazole → N-(2-chloro-5-thiazolylmethyl)-N'-methyl-N"-nitroguanidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-5-aminomethylthiazole | HCID 10154129 | — |
| Reactant | 1,2-Dimethyl-3-nitroisothiourea | HCID 136227017 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(2-chloro-5-thiazolylmethyl)-N'-methyl-N"-nitroguanidine | HCID 135779804 | 71.3% |
Reaction Steps
A mixture of 0.48 g of 2-chloro-5-thiazolemethanamine, 0.31 g of S-methyl-N-methyl-N'-nitroisothiourea prepared by the method described in the Journal of Medical Chemistry., 1977, Vol. 20, No. 7, P. 905 and 3 ml of ethanol was heated under reflux for 6 hours. After cooling, the reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (Solvent: Chloroform/Methanol =20/1) to obtain 0.37 g of the title compound as crystals. This compound is No. 8 in Table 1. m.p.: 151.0°-153.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05166164 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-49f0d7f98ad84f98adfa15b26181d2ec |
| Source note | uspto-grants-1992_11 |