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HRID 79191作成日:2026年10月26日

Cyclopentylamine → N4-cyclopentylpyrimidine-2,4-diamine

https://huagongshe.com/reaction/79191

反応式

関与物質

役割名称HCID仕込み量
反応物CyclopentylamineHCID 2906—
反応物TriethylamineHCID 8471—
反応物2-Amino-4-chloropyrimidineHCID 223332—
溶媒EthanolHCID 702—
生成物N4-cyclopentylpyrimidine-2,4-diamineHCID 5829989084.5%

反応条件

温度105 °C

反応手順

A mixture of 2-amino-4-chloropyrimidine (22.8 g, 176 mmol), cyclopentylamine (20.9 mL, 211 mmol) and triethylamine (29.4 mL, 211 mmol) in EtOH (200 mL) was heated at reflux (105° C., oil bath) for 48 h. Upon workup, the volatile was removed in vacuo. The residue was poured into ice and saturated Na2CO3 aqueous solution and extracted with ethyl acetate (3×). The combined organics were washed with saturated Na2CO3 aqueous solution (1×), dried over Na2SO4, and concentrated in vacuo to give N4-cyclopentylpyrimidine-2,4-diamine (315) (26.5 g) as a light yellow solid of 92% purity. This batch of material was taken onto the next step without further purification. LCMS-ESI (POS), M/Z, M+1: Found 179.1, Calculated 179.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841312B2
出典データセットuspto-grants-2014_09
ORD IDord-50f69fdebf1f4b2284aa376c6e2cf73c
出典メモuspto-grants-2014_09