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HRID 746430作成日:2026年10月25日

N-(3,5-dichloropyrid-4-yl)-4-difluoromethoxy-8-nitro-dibenzo[b,d]furan-1-carboxamide → N-(3,5-dichloropyrid-4-yl)-4-difluoromethoxy-8-amino-dibenzo[b,d]furan-1-carboxamide

https://huagongshe.com/reaction/746430

反応式

関与物質

役割名称HCID仕込み量
反応物N-(3,5-dichloropyrid-4-yl)-4-difluoromethoxy-8-nitro-dibenzo[b,d]furan-1-carboxamideHCID 10050271—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物N-(3,5-dichloropyrid-4-yl)-4-difluoromethoxy-8-amino-dibenzo[b,d]furan-1-carboxamideHCID 10320896—

反応手順

A mixture of N-(3,5-dichloropyrid-4-yl)-4-difluoromethoxy-8-nitro-dibenzo[b,d]furan-1-carboxamide (step 8) (100 mg), methanol (10 ml) and 10% Pd/C (10 mg) was hydrogenated at 60 psi for 12 h. Filteration of the reaction mixture over celite bed and removal of solvent methanol under reduced pressure afforded N-(3,5-dichloropyrid-4-yl)-4-difluoromethoxy-8-amino-dibenzo[b,d]furan-1-carboxamide as white solid. mp: >270° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07393846B2
出典データセットuspto-grants-2008_07
ORD IDord-c7beb921ce3647ab8bad29f62514dc91
出典メモuspto-grants-2008_07