돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1372644생성일: 2026년 10월 26일

5-Fluoro-o-tolyl Isothiocyanate → Methyl (2-(5-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetate

https://huagongshe.com/reaction/1372644

반응식

참여 물질

역할이름HCID투입량
반응물5-Fluoro-o-tolyl IsothiocyanateHCID 519443—
반응물Methyl (4-amino-2-fluoro-3-hydroxyphenyl)acetateHCID 17859032—
용매MethanolHCID 887—
생성물Methyl (2-(5-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetateHCID 4460752156%

반응 단계

In methanol (30 ml) was dissolved methyl (4-amino-2-fluoro-3-hydroxyphenyl)acetate (1.0 g, 5.02 mmol). To the resulting solution was added 5-fluoro-2-methylphenyl isothiocyanate (1.0 g, 5.98 mmol). After the resulting mixture was stirred at room temperature for 5 days, mercuric oxide (yellow) (1.14 g, 4.36 mmol) was added thereto. The mixture was stirred at 70° C. for 6 hours. After cooling to room temperature, the reaction mixture was filtered through Celite and washed with methanol. The filtrate was distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from chloroform/ethyl acetate (30/1, v/v) eluate fractions, methyl (2-(5-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetate (810 mg, 56% (2 steps)) was obtained as a pink solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07157487B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-672c550ec85c4431afa5341f70e99fc0
출처 메모uspto-grants-2007_01