HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → O-methyl-N-(2-chloro-5-thiazolylmethyl)-N'-nitroisourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chloro-5-aminomethylthiazole | HCID 10154129 | — |
| Reactant | O-methyl-N-nitroisourea | HCID 136196430 | — |
| Solvent | Water | HCID 962 | — |
| Product | O-methyl-N-(2-chloro-5-thiazolylmethyl)-N'-nitroisourea | HCID 136404632 | 46% |
Reaction Steps
O-methyl-N-nitroisourea (3.0 g, 0.0252 mol), acetic acid (1.5 ml, 0.0262 mol, 10.4 equivalents), and 5-(aminomethyl)-2-chlorothiazole (93% purity, 4.4 g, 0.0275 mol, 1.09 equivalents) were added to water (55 ml) in this order at 24° C. The reaction mixture was adjusted to pH 7 with 30% aqueous sodium hydroxide solution. The mixture was stirred at room temperature for 2 hours and then extracted with dichloromethane. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to provide 2.9 g (46.0% yield) of O-methyl-N-(2-chloro-5-thiazolylmethyl)-N'-nitroisourea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06008363 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-c7a6f3442714478a8d48e5bfc1a3fa6b |
| Source note | uspto-grants-1999_12 |