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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8617생성일: 2026년 10월 24일

Sodium hydride → 2-Phenyl-ethanesulfonic acid {5-p-tolyl-6-[2-(5-trifluoromethyl-pyridin-2-yloxy)-ethoxy]-pyrimidin-4-yl}-amide

https://huagongshe.com/ko/reaction/8617

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2-Chloro-5-(trifluoromethyl)pyridineHCID 92342—
반응물2-Phenyl-ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-p-tolyl-pyrimidin-4-yl]-amideHCID 23548269—
용매TetrahydrofuranHCID 8028—
생성물2-Phenyl-ethanesulfonic acid {5-p-tolyl-6-[2-(5-trifluoromethyl-pyridin-2-yloxy)-ethoxy]-pyrimidin-4-yl}-amideHCID 2354824588.8%

반응 단계

To sodium hydride (27 mg, 60% in mineral oil) was added THF (15 ml) followed by 2-phenyl-ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-p-tolyl-pyrimidin-4-yl]-amide (80 mg, Referential Example 1). The mixture was stirred for 1 h at rt before 2-chloro-5-trifluoromethyl-pyridine (86 mg) was added. Stirring was continued for 17 h at 80° C. The solvent was evaporated, the residue was dissolved in water (20 ml), acidified with citric acid. The suspension was treated with hexane (15 ml). The solid material was collected, washed with hexane:EA 1:1 (20 ml) and dried to yield 2-phenyl-ethanesulfonic acid {5-p-tolyl-6-[2-(5-trifluoromethyl-pyridin-2-yloxy)-ethoxy]-pyrimidin-4-yl}-amide (96 mg) as beige powder. LC-MS: tR=5.86 min, [M+1]+=559.20, [M−1]−=557.37.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091201B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-7ba9c64b1ade4f3bbbe979f0ff322f01
출처 메모uspto-grants-2006_08