돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2352460생성일: 2026년 10월 27일

Methyl 4-ethoxy-2-(isocyanatosulfonyl)benzoate → Methyl 2-[[[4-(difluoromethoxy)-6-methoxypyrimidin-2-yl]aminocarbonyl]aminosulfonyl]-4-ethoxybenzoate

https://huagongshe.com/reaction/2352460

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 4-ethoxy-2-(isocyanatosulfonyl)benzoateHCID 13987873—
반응물4-Difluoromethoxy-6-methoxypyrimidin-2-amineHCID 14695654—
용매DichloromethaneHCID 6344—
생성물Methyl 2-[[[4-(difluoromethoxy)-6-methoxypyrimidin-2-yl]aminocarbonyl]aminosulfonyl]-4-ethoxybenzoateHCID 14695655—

반응 단계

To a slurry of 4-difluoromethoxy-6-methoxypyrimidin-2-amine (0.56 g, 2.92 mmol) in dry dichloromethane (5 mL) was added a solution of methyl 4-ethoxy-2-(isocyanatosulfonyl)benzoate (crude, ca. 5.6 mL) in dichloromethane (5 mL). The reaction mixture was heated at reflux for 3 hours, during which time the solid dissolved. On stirring at room temperature for 12 hours a new solid formed. The crude reaction mixture was chromatographed directly on a column of silica gel using as eluant 40:1, 20:1, and finally 10:1 dichloromethane-ether, all containing 2 mL/L acetic acid. The appropriate fractions were diluted with toluene and rotary evaporated to give a solid. The solid was slurried in hexanes, collected, washed with butyl chloride, 1:1 butyl chloride-hexanes, hexanes and air dried. The product was a white crystalline solid melting at 195°-196° C. PMR (CDCl3, 200 MHz): δ 12.02 (bs, 1H); 7.91 (d, 1H); 7.78 (d, 1H); 7.52 (t, 1H); 7.34 (bs, 1H); 7.09 (dd, 1H); 5.97 (s, 1H); 4.17 (q, 2H); 4.12 (s, 3H); 3.87 (s, 3H); 1.46 (t, 3H). IR (Nujol): 1722 (vs, C=O) cm-1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04877442
출처 데이터셋uspto-grants-1989_10
ORD IDord-751080ef335f47a0adacf464ed0300de
출처 메모uspto-grants-1989_10