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HRID 15369作成日:2026年10月26日

Tetrafluoro-m-phenylenediamine dihydrochloride → (4r)-4-({4-[(2,3-Dihydro-1,4-benzodioxin-6-ylmethyl)amino]-1-piperidinyl}methyl)-3-fluoro-4,5-dihydro-7h-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one dihydrochloride

https://huagongshe.com/reaction/15369

反応式

関与物質

役割名称HCID仕込み量
反応物Tetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
反応物2,3-Dihydro-1,4-benzodioxin-6-carbaldehydeHCID 248127—
反応物(4R)-4-[(4-amino-1-piperidinyl)methyl]-3-fluoro-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-oneHCID 68686964—
生成物(4r)-4-({4-[(2,3-Dihydro-1,4-benzodioxin-6-ylmethyl)amino]-1-piperidinyl}methyl)-3-fluoro-4,5-dihydro-7h-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one dihydrochlorideHCID 6868483771%

反応手順

The title compound was prepared from (4R)-4-[(4-amino-1-piperidinyl)methyl]-3-fluoro-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one Enantiomer 1 and 2,3-dihydro-1,4-benzodioxin-6-carboxaldehyde (Aldrich) according to the general method of Example 2(h) (except that the dihydrochloride was prepared) in 71% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732461B2
出典データセットuspto-grants-2010_06
ORD IDord-2ed63c1b192a4d2ead674ec3f2add09b
出典メモuspto-grants-2010_06