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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1719499생성일: 2026년 10월 27일

5-Amino-2-hydroxy-2,4,6-cycloheptatrien-1-one → 4-hydroxy-2-methyl-N-(2-hydroxy-1-oxo-2,4,6-cycloheptatrien-5-yl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide

https://huagongshe.com/reaction/1719499

반응식

참여 물질

역할이름HCID투입량
반응물5-Amino-2-hydroxy-2,4,6-cycloheptatrien-1-oneHCID 23450—
반응물methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxideHCID 54676532—
용매O-XyleneHCID 7237—
생성물4-hydroxy-2-methyl-N-(2-hydroxy-1-oxo-2,4,6-cycloheptatrien-5-yl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxideHCID 5471269753.3%

반응 단계

In a nitrogen atmosphere, a solution of methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide (0.54 g) and 5-amino-2-hydroxy-2,4,6 -cycloheptatrien-1-one (0.33 g) in xylene (15 ml) is refluxed for 7.5 hours. The reaction mixture is then allowed to stand at room temperature overnight. The crystals that have separated out are collected by filtration and recrystallized from dimethylformamidemethanol to give 4-hydroxy-2-methyl-N-(2-hydroxy-1-oxo-2,4,6-cycloheptatrien-5-yl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide (0.4 g), m.p. 258°-265° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04540692
출처 데이터셋uspto-grants-1985_09
ORD IDord-692ec9fc08ed41e7982363ce4136aff3
출처 메모uspto-grants-1985_09