HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylic acid → 3-(3-chloro-1H-pyrazol-1-yl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylic acid | HCID 91754480 | — |
| Catalyst | Copper oxide | HCID 14829 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(3-chloro-1H-pyrazol-1-yl)pyridine | HCID 67499540 | — |
Reaction Steps
In step d of Scheme 2, 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylic acid (6e) is decarboxylated in the presence of copper (II) oxide in polar solvents such as N,N-dimethylformamide at temperatures from about 80° C. to about 140° C. to yield 3-(3-chloro-1H-pyrazol-1-yl)pyridine (5b). It was surprisingly discovered that this decarboxylation only occurs in the presence of copper (II) oxide. Several known decarboxylation agents from the literature such as, for example, hydrochloric acid (See alternate synthetic route, Example 14), sulfuric acid, and palladium (II) trifluoroacetate/trifluoroacetic acid (Pd(TFA)2/TFA) (See “CE-5”) did not yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09434712B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-1a23c4ccebed4846af0dbda241626759 |
| Source note | uspto-grants-2016_09 |