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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8593생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/8593

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4,6-Dichloro-5-(4-methylphenyl)pyrimidineHCID 21979554—
반응물2-Phenyl-ethanesulfonic acid amide potassium saltHCID 68898150—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물2-Phenyl-ethanesulfonic acid (6-chloro-5-p-tolyl-pyrimidin-4-yl)-amideHCID 8659246959.6%

반응 조건

온도5 °C

반응 단계

A solution of 2-phenyl-ethanesulfonic acid amide potassium salt (3.0 g), 4,6-dichloro-5-p-tolyl-pyrimidine (2.15 g) and Hunig's base (1.57 ml) in DMSO (50 ml) was stirred at rt for 20 h before it was diluted with water (500 ml) and extracted twice with diethyl ether (250 ml). The aqueous phase was acidified with acetic acid. The resulting suspension was cooled to 5° C. and filtered. The solid material was washed with water and diethyl ether, and dried at 40° C. under high vacuum to give 2-phenyl-ethanesulfonic acid (6-chloro-5-p-tolyl-pyrimidin-4-yl)-amide (2.08 g) as a grey powder. LC-MS: tR=5.23 min, [M+1]+=388.18, [M−1]−=386.14.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091201B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-de2c64610930487e978e7f18ba39fabb
출처 메모uspto-grants-2006_08