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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Phosphorus oxychloride | HCID 24813 | — |
| 반응물 | 1-(2,4-difluorophenyl)-1-(4-(4-carbamoylthiazol-2-yl)-thiophen-2-yl)-2-(1H-1,2,4-triazol-1-yl)ethanol | HCID 19065156 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | 1-(2,4-difluorophenyl)-1-(4-(4-cyanothiazol-2-yl)-thiophen-2-yl)-2-(1H-1,2,4-triazol-1-yl)ethanol | HCID 19065151 | 69.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05789429 |
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| 출처 데이터셋 | uspto-grants-1998_08 |
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| ORD ID | ord-bba6c4fbdb8240a88b9f3cdfa9b7539e |
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| 출처 메모 | uspto-grants-1998_08 |
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