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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 483024생성일: 2026년 10월 26일

Dicyclohexylcarbodiimide → benzotriazol-1-yl (2Z)-2-methoxyimino-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetate

https://huagongshe.com/reaction/483024

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acidHCID 5928144—
용매TetrahydrofuranHCID 8028—
생성물benzotriazol-1-yl (2Z)-2-methoxyimino-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetateHCID 8867599193%

반응 단계

To a solution of 2-(2-tritylaminothiazol-4-yl)-(Z)-2-methoxyiminoacetic acid (2.22 g, 5 mmol) and 1-hydroxybenzotriazole (0.74 g, 5.5 mmol) in tetrahydrofuran (22 ml) was added N,N'-dicyclohexylcarbodiimide (1.14 g, 5.5 mmol) at 5°-10° C. and the mixture was stirred at the same temperature for 3 hours. Precipitated N,N'-dicyclohexylurea was removed by filtration and the filtrate was concentrated under reduced pressure. The residue was dissolved in chloroform (20 ml) and insoluble material was removed by filtration. The chloroform was evaporated and the residue was treated with a small quantity of ether to give colorless needles of 1-benzotriazolyl 2-(2-tritylaminothiazol-4-yl)-(Z)-2-methoxyiminoacetate (2.60 g, 93%), mp 178°-179° C. (decomposition).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04576938
출처 데이터셋uspto-grants-1986_03
ORD IDord-de584faa82294b62aa037648a02c0640
출처 메모uspto-grants-1986_03