HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 4-(6-(Acetamidomethyl)pyridin-2-yl)-2-guanidinothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(6-Aminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole | HCID 10399768 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-(6-(Acetamidomethyl)pyridin-2-yl)-2-guanidinothiazole | HCID 10446940 | — |
Reaction Steps
Acetic anhydride was added dropwise to a solution of 4-(6-aminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole (0.44 g) in pyridine (4.4 ml). After being stirred for two hours at ambient temperature, the mixture was mixed with aqueous potassium carbonate and extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and evaporated in vacuo to give 4-(6-acetylaminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole. The residue was converted to the hydrochloride in a usual manner and the salt was recrystallized from a mixture of methanol and diisopropyl ether to give 4-(6-acetylaminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole dihydrochloride (0.43 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05371097 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-f9c3e787bb824cb1aab2bf913dce7a17 |
| Source note | uspto-grants-1994_12 |