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HRID 18477作成日:2026年10月24日

2H-Pyran-3(4H)-one, dihydro- → 3-(2,4,5-Trifluorophenyl)-1,4,5,7-tetrahydropyrano[3,4-c]pyrazole

https://huagongshe.com/ja/reaction/18477

反応式

関与物質

役割名称HCID仕込み量
反応物2H-Pyran-3(4H)-one, dihydro-HCID 90109—
反応物2,4,5-Trifluorobenzoyl chlorideHCID 145164—
反応物tert-butyl 3-(3,4-difluorophenyl)-6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxylateHCID 59345327—
生成物3-(2,4,5-Trifluorophenyl)-1,4,5,7-tetrahydropyrano[3,4-c]pyrazoleHCID 59345342—

反応手順

Intermediate 16D was prepared according to the procedure for the synthesis of intermediate 15 by replacing 1-Boc-4-piperidone with dihydro-2H-pyran-3(4H)-one, and replacing 3,4-difluorobenzoyl chloride with 2,4,5-trifluorobenzoyl chloride. LCMS (+ESI) m/z=255 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741350B1
出典データセットuspto-grants-2010_06
ORD IDord-36dedcaa54664e099a65833376c16631
出典メモuspto-grants-2010_06