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HRID 361864作成日:2026年10月26日

Triethylamine → 1-Benzyl-4-[N-ethyl-N-(6-chloro-5-nitro-4-pyrimidinyl)amino]piperidine

https://huagongshe.com/reaction/361864

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4,6-Dichloro-5-nitropyrimidineHCID 20312—
反応物Sodium BicarbonateHCID 516892—
反応物1-Benzyl-4-[N-ethyl-N-(3-(ethylamino)-2-pyridinyl)amino]piperidineHCID 10497248—
溶媒DichloromethaneHCID 6344—
生成物1-Benzyl-4-[N-ethyl-N-(6-chloro-5-nitro-4-pyrimidinyl)amino]piperidineHCID 54473155—

反応手順

4,6-Dichloro-5-nitropyrimidine (8.88 g) is dissolved in 400 ml of methylene chloride and cooled to -78°. Then triethylamine (6.7 ml) and 1-benzyl-4-N-ethylaminopiperidine (EXAMPLE 205, 10.00 g) is added and the reaction is stirred 1 hr at -78° and slowly warmed to 20°-25°. The reaction is poured into saturated aqueous sodium bicarbonate, extracted with methylene chloride, washed with saline, dried and concentrated under reduced pressure. Purification by flash column chromatography (10% ethyl acetate/hexane to 50% ethyl acetate/hexane) gives the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05866589
出典データセットuspto-grants-1999_02
ORD IDord-4edf6c954f5d40a1a38d8709acd6c1fe
出典メモuspto-grants-1999_02