HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-[1-(6-Chloro-2-pyridyl)-2-pyrazolin-3-yl]formamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | N-[1-(6-Chloro-2-pyridyl)-2-pyrazolin-3-yl]acetamide | HCID 13050983 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | N-[1-(6-Chloro-2-pyridyl)-2-pyrazolin-3-yl]formamide | HCID 13050984 | — |
Reaction Steps
A mixture of 5.0 g. of 2-(3-amino-2-pyrazolin-1-yl)-6-chloropyridine (prepared as described in Example 3) and 25 ml. of a mixture of formic acid and acetic anhydride (Feiser and Feiser, Reagents for Organic Synthesis, Vol. 1, page 4) at room temperature gives an immediate yellow precipitate. The precipitate is collected by filtration then is recrystallized from acetone-hexane to give 3.05 g. of the product of the Example as off-white crystals, m.p. 190°-192° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04347251 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-b3c9d641736e4e999de7ec8af81e9585 |
| Source note | uspto-grants-1982_08 |