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HRID 44804作成日:2026年10月25日

(R)-Methyl 2-((2-chloro-5-nitropyrimidin-4-yl)(cyclopentyl)amino)butanoate → (R)-methyl 2-((2-chloro-5-nitropyrimidin-4-yl)(isopropyl)amino)butanoate

https://huagongshe.com/reaction/44804

反応式

関与物質

役割名称HCID仕込み量
反応物(R)-Methyl 2-((2-chloro-5-nitropyrimidin-4-yl)(cyclopentyl)amino)butanoateHCID 58405447—
溶媒AcetoneHCID 180—
生成物(R)-methyl 2-((2-chloro-5-nitropyrimidin-4-yl)(isopropyl)amino)butanoateHCID 59815009—

反応手順

Intermediate C-1 was prepared similarly to the synthetic methods used to prepare Intermediate A with the exception that acetone was used instead of cyclopentanone in the reductive amination step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541418B2
出典データセットuspto-grants-2013_09
ORD IDord-3fd893af0d6544c4821cd0d1f8d7b325
出典メモuspto-grants-2013_09