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HRID 57084作成日:2026年10月26日

3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylic acid → 3-(3-chloro-1H-pyrazol-1-yl)pyridine

https://huagongshe.com/reaction/57084

反応式

関与物質

役割名称HCID仕込み量
反応物3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylic acidHCID 91754480—
触媒Copper oxideHCID 14829—
溶媒DimethylformamideHCID 6228—
生成物3-(3-chloro-1H-pyrazol-1-yl)pyridineHCID 67499540—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434712B2
出典データセットuspto-grants-2016_09
ORD IDord-1a23c4ccebed4846af0dbda241626759
出典メモuspto-grants-2016_09