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HRID 1471778作成日:2026年10月26日

4-(N-Ethylaminocarbonyl)phenylboronic acid → 4-[5-(4-Ethylcarbamoyl-phenyl)-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1471778

反応式

関与物質

役割名称HCID仕込み量
反応物4-(N-Ethylaminocarbonyl)phenylboronic acidHCID 3411307—
反応物4-(5-Chlorofuro[2,3-c]pyridin-2-yl)piperidine-1-carboxylic acid tert-butyl esterHCID 86674889—
生成物4-[5-(4-Ethylcarbamoyl-phenyl)-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl esterHCID 71736416—

反応手順

The title compound is prepared from 4-(5-chloro-furo[2,3-c]pyridin-2-yl)-piperidine-1-carboxylic acid tert-butyl ester and 4-ethylcarbamoyl-phenylboronic acid following a procedure analogous to that described for Example 1; the reaction is conducted at 150° C. LC (method 4): tR=1.68 min; Mass spectrum (ESI+): m/z=450 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09012456B2
出典データセットuspto-grants-2015_04
ORD IDord-84755c5c51e145e583c4e8701482eec7
出典メモuspto-grants-2015_04