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HRID 30085作成日:2026年10月25日

Diphenyl N-Cyanocarbonimidate → Phenyl N-cyano-N'-(2-{[4-(2,4-difluorophenyl)-8-(2-fluorophenyl)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidin-2-yl]amino}ethyl)imidocarbamate

https://huagongshe.com/reaction/30085

反応式

関与物質

役割名称HCID仕込み量
反応物Diphenyl N-CyanocarbonimidateHCID 688090—
反応物2-[(2-Aminoethyl)amino]-4-(2,4-difluorophenyl)-8-(2-fluorophenyl)pyrido[2,3-d]pyrimidin-7(8H)-oneHCID 59789333—
溶媒IsopropanolHCID 3776—
生成物Phenyl N-cyano-N'-(2-{[4-(2,4-difluorophenyl)-8-(2-fluorophenyl)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidin-2-yl]amino}ethyl)imidocarbamateHCID 59789332—

反応条件

温度20 °C

反応手順

To a solution of 2-[(2-aminoethyl)amino]-4-(2,4-difluorophenyl)-8-(2-fluorophenyl)pyrido[2,3-d]pyrimidin-7(8H)-one (28 mg, 0.070 mmol) in isopropanol (2 mL) was added diphenyl cyanocarbonimidate (17 mg, 0.070 mmol). The mixture was stirred for about 30 min at about 20° C. LC/MS showed a new peak corresponding to the desired product and no starting material in the solution. LC-MS m/z 556 (M+H)+, 3.24 min (ret time).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423042B2
出典データセットuspto-grants-2008_09
ORD IDord-83e404ccb1e94720998b7aad81cd5039
出典メモuspto-grants-2008_09