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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 481560생성일: 2026년 10월 25일

Phosphorus oxychloride → 1-(2,4-difluorophenyl)-1-(4-(4-cyanothiazol-2-yl)-thiophen-2-yl)-2-(1H-1,2,4-triazol-1-yl)ethanol

https://huagongshe.com/reaction/481560

반응식

참여 물질

역할이름HCID투입량
반응물Phosphorus oxychlorideHCID 24813—
반응물1-(2,4-difluorophenyl)-1-(4-(4-carbamoylthiazol-2-yl)-thiophen-2-yl)-2-(1H-1,2,4-triazol-1-yl)ethanolHCID 19065156—
용매PyridineHCID 1049—
생성물1-(2,4-difluorophenyl)-1-(4-(4-cyanothiazol-2-yl)-thiophen-2-yl)-2-(1H-1,2,4-triazol-1-yl)ethanolHCID 1906515169.6%

반응 단계

1-(2,4-Difluorophenyl)-1-(4-(4-carbamoylthiazol-2-yl)-thiophen-2-yl)-2-(1H-1,2,4-triazol-1-yl)ethanol (1.2 g) was dissolved in pyridine (7.1 ml). The solution was cooled on an ice bath, and phosphorus oxychloride (0.29 ml) was added thereto. The resultant mixture was stirred for 30 minutes. After the reaction, the reaction mixture was added with saline and extracted with ethyl acetate. An organic layer was washed once with 6N hydrochloric acid (20 ml) and then each once with water, a saturated aqueous solution of sodium hydrogencarbonate and saturated saline. After the thus-washed organic layer was dried over magnesium sulfate, the solvent was distilled out, and the residue was purified by chromatography on silica gel. Recrystallization from a solution of dichloromethane in ether was further conducted to obtain a solid (800 mg). Melting point: 172°-173° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05789429
출처 데이터셋uspto-grants-1998_08
ORD IDord-bba6c4fbdb8240a88b9f3cdfa9b7539e
출처 메모uspto-grants-1998_08