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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 542250생성일: 2026년 10월 26일

Phosgene → 5-Methyl-3-(2-pyridyl)-2H,5H-1,3-oxazino-[5,6-c] thieno[2,3-e] 1,2-thiazine-2,4-(3H)-dione 6,6-dioxide hydrochloride

https://huagongshe.com/reaction/542250

반응식

참여 물질

역할이름HCID투입량
반응물PhosgeneHCID 6371—
반응물TriethylamineHCID 8471—
반응물TenoxicamHCID 54677971—
용매TolueneHCID 1140—
생성물5-Methyl-3-(2-pyridyl)-2H,5H-1,3-oxazino-[5,6-c] thieno[2,3-e] 1,2-thiazine-2,4-(3H)-dione 6,6-dioxide hydrochlorideHCID 20209820—

반응 단계

To a solution of 3.37 g. (10 mmole) N-(2-pyridyl)-4-hydroxy-2-methyl-2H-thieno[2,3-e]-1,2-thiazine-3-carboxamide 1,1-dioxide (tenoxicam) in 150 ml. toluene under nitrogen is added 1.01 g. (10 mmole) triethylamine and the mixture is cooled to 0° C. The cold solution is then added dropwise to a solution of 1.0 g. (10 mmole) phosgene in 50 ml. toluene at -70° C. over 45 minutes and stirring is continued at -70° to -60° C. for an additional 30 minutes. The reaction mixture is allowed to warm to room temperature and stirred for an hour. The solvent is evaporated in vacuo, the residue triturated with acetone and filtered to obtain the desired product which is purified by recrystallization, e.g., from acetine, ethanol or chloroform.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04656265
출처 데이터셋uspto-grants-1987_04
ORD IDord-b971470fe1ed433b816949f64be0e5c7
출처 메모uspto-grants-1987_04