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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1438606생성일: 2026년 10월 26일

8-{5-Chloro-3-[(4-chloro-3-trifluoromethyl-benzenesulfonyl)-methoxymethyl-amino]-pyridine-2-carbonyl}-2,3-dihydro-benzo[1,4]oxazine-4-carboxylic acid tert-butyl ester → 3-(Trifluoromethyl)benzene-1-sulfonamide

https://huagongshe.com/reaction/1438606

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참여 물질

역할이름HCID투입량
반응물8-{5-Chloro-3-[(4-chloro-3-trifluoromethyl-benzenesulfonyl)-methoxymethyl-amino]-pyridine-2-carbonyl}-2,3-dihydro-benzo[1,4]oxazine-4-carboxylic acid tert-butyl esterHCID 66649061—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
생성물3-(Trifluoromethyl)benzene-1-sulfonamideHCID 244076123.8%

반응 단계

A solution of 8-{5-chloro-3-[(4-chloro-3-trifluoromethyl-benzenesulfonyl)-methoxymethyl-amino]-pyridine-2-carbonyl}-2,3-dihydro-benzo [1,4]oxazine-4-carboxylic acid tert-butyl ester (510.2 mg) in 3 mL HCl (4 M in dioxane) and water (1 mL) was heated at 80 OC for overnight. Upon cooling to room temperature, the mixture was concentrated and the residue was purified by flash column chromatography on silica gel to afford 4-chloro-NJ5-chloro-2-(3,4-dihydro-2H-benzo[1,4]oxazine-8-carbonyl)-pyridin-3-yl]-3-trifluoromethyl-benzenesulfonamide (210.2 mg) as white solid. MS m/z: 531.9 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07622583B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-fb07e624f6e54ff9ac3d17df4ee4ab20
출처 메모uspto-grants-2009_11