돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 703038생성일: 2026년 10월 26일

Tetrahydrofuran → 3-[2-Methyl-3,4-dihydro-3-oxo-4-(propynyl)-2H-1,4-benzoxazin-6-yl]-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione

https://huagongshe.com/reaction/703038

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Sodium hydrideHCID 24758—
반응물Ethyl 3-amino-4,4,4-trifluoro-2-butenoateHCID 136209—
반응물6-isocyanato-2-methyl-3,4-dihydro-3-oxo-4-(2-propynyl)-2H-1,4-benzoxazineHCID 15029563—
용매Acetic AcidHCID 176—
생성물3-[2-Methyl-3,4-dihydro-3-oxo-4-(propynyl)-2H-1,4-benzoxazin-6-yl]-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedioneHCID 22151123—

반응 조건

온도-70 °C

반응 단계

A slurry of 1.4 g. of sodium hydride in 25 ml. of dry tetrahydrofuran (THF) was cooled to -10° C. To the cooled and stirred slurry was added a solution of 10.0 g. of ethyl 3-amino-4,4,4-trifluoro-2-butenoate in 50 ml. of THF. The addition of this solution was made over a period of 30 minutes. The resultant light brown reaction mixture was cooled to -70° C. A solution of 13.3 g. of 6-isocyanato-2- methyl-3,4-dihydro-3-oxo-4-(2-propynyl)-2H-1,4-benzoxazine in 75 ml. of THF was added to the chilled reaction mixture over a period of 10 minutes. After stirring at -70° C. for 30 minutes, the temperature was allowed to rise slowly to 10° C. At that point 3.6 ml. of acetic acid was added to the mixture. A beige solid precipitated. 19.0 Grams of the solid was recovered by filtering it from the reaction mixture.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04981508
출처 데이터셋uspto-grants-1991_01
ORD IDord-d05d21b41e2b446ba3921ae65d778a14
출처 메모uspto-grants-1991_01