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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8596생성일: 2026년 10월 24일

Diisopropylethylamine → 2-Phenyl-ethanesulfonic acid (6-chloro-2-pyridin-4-yl-5-p-tolyl-pyrimidin-4-yl)-amide

https://huagongshe.com/ko/reaction/8596

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4,6-Dichloro-2-(4-pyridyl)-5-(p-tolyl)-pyrimidineHCID 21979575—
반응물2-Phenyl-ethanesulfonic acid amide potassium saltHCID 68898150—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물2-Phenyl-ethanesulfonic acid (6-chloro-2-pyridin-4-yl-5-p-tolyl-pyrimidin-4-yl)-amideHCID 8659247021.8%

반응 단계

A solution of 4,6-dichloro-2-(4-pyridyl)-5-(p-tolyl)-pyrimidine (1.5 g), 2-phenyl-ethanesulfonic acid amide potassium salt (1.44 g, Referential Example 1e) and Hunig's base (1 ml) in DMSO (20 ml) was stirred at rt for 24 h before it was diluted with water (150 ml) and extracted twice with diethyl ether. The aqueous layer was acidified with acetic acid. The precipitate was collected, and further purified by column chromatography on silica gel eluting with hexane:EA 1:1 to give 2-phenyl-ethanesulfonic acid (6-chloro-2-pyridin-4-yl-5-p-tolyl-pyrimidin-4-yl)-amide (480 mg) as a foam. LC-MS: tR=5.08 min, [M+1]+=465.13, [M−1]−=462.96.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091201B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b939b42b0d324149bc288dcb9f098465
출처 메모uspto-grants-2006_08