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HRID 1522087作成日:2026年10月25日

Diisopropylethylamine → HCID 71092810、化合物

https://huagongshe.com/reaction/1522087

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物1-Boc-4-(aminomethyl)piperidineHCID 736817—
反応物5,6-Dichloro-pyrimidin-4-ylamineHCID 24219262—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物HCID 71092810HCID 71092810—

反応手順

Into a 10-mL vial was placed 5,6-dichloropyrimidin-4-amine (250.00 mg; 1.52 mmol), tert-butyl 4-(aminomethyl)piperidine-1-carboxylate (653.40 mg; 3.05 mmol), and N,N-diisopropylethylamine (1.01 ml; 6.10 mmol) suspended in NMP (2.50 ml). The reaction mixture was run in the microwave at 150° C. for 2 hours. The reaction mixture was allowed to cool to rt. The mixture was purified using Biotage column chromatography eluting from 50-100% EtOAc/Hexanes. Fractions containing the desired product were combined and concentrated under reduced pressure to afford tert-butyl 4-{[(6-amino-5-chloropyrimidin-4-yl)amino]methyl}piperidine-1-carboxylate as a yellow viscous oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09073947B2
出典データセットuspto-grants-2015_07
ORD IDord-a88b0fd9e26b458ca627e84b7842006a
出典メモuspto-grants-2015_07