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HRID 2409164作成日:2026年10月26日

2-Methyl-1H-imidazole-4-carboxaldehyde → (S)-2-Amino-6-{2-fluoro-5-[(2-methyl-3H-imidazol-4-ylmethyl)-amino]-phenyl}-3,5,5,6-tetramethyl-5,6-dihydro-3H-pyrimidin-4-one

https://huagongshe.com/reaction/2409164

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-1H-imidazole-4-carboxaldehydeHCID 2795878—
反応物(S)-2-amino-6-(5-amino-2-fluoro-phenyl)-3,5,5,6-tetramethyl-5,6-dihydro-3H-pyrimidin-4-oneHCID 57497157—
反応物HCID 178419135HCID 178419135—
生成物(S)-2-Amino-6-{2-fluoro-5-[(2-methyl-3H-imidazol-4-ylmethyl)-amino]-phenyl}-3,5,5,6-tetramethyl-5,6-dihydro-3H-pyrimidin-4-oneHCID 57497081—

反応手順

The reductive amination of (S)-2-amino-6-(5-amino-2-fluoro-phenyl)-3,5,5,6-tetramethyl-5,6-dihydro-3H-pyrimidin-4-one (intermediate J) and 2-methyl-3H-imidazole-4-carbaldehyde using decaborane yielded the title compound as a white solid. MS (ESI): m/z=373.2 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08815881B2
出典データセットuspto-grants-2014_08
ORD IDord-af97d473a6384e9fa054a926d8aa7400
出典メモuspto-grants-2014_08