HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Chloro-thiazol-5-ylmethyl)-methyl-amine → N-[(2-chloro-5-thiazolyl)methyl]-N-methyl-N'-nitroguanidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Chloro-thiazol-5-ylmethyl)-methyl-amine | HCID 22450372 | — |
| Reactant | N-Nitro-S-methylisothiourea | HCID 135927615 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[(2-chloro-5-thiazolyl)methyl]-N-methyl-N'-nitroguanidine | HCID 136023519 | 47.9% |
Reaction Steps
A mixture of 1.50 g of 2-chloro-N-methyl-5-thiazolemethanamine, 1.13 g of S-methyl-N-nitroisothiourea and 6 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 1.00 g of the title compound as crystals. This compound is No. 6 in Table 1. m.p.: 116.0°-117.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05166164 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-413423d140104099ae13a250c643f00b |
| Source note | uspto-grants-1992_11 |