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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1391825생성일: 2026년 10월 25일

Triethylamine → sodium (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[(2-methyl-5,6-dioxo-1H-1,2,4-triazin-3-yl)sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

https://huagongshe.com/reaction/1391825

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium AcetateHCID 517045—
반응물HCID 178502822HCID 178502822—
용매AcetoneHCID 180—
생성물sodium (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[(2-methyl-5,6-dioxo-1H-1,2,4-triazin-3-yl)sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylateHCID 178502823—

반응 단계

The ceftriaxone acid was dissolved in aqueous acetone using triethylamine. To the clear solution obtained, sodium acetate (13 g) was added and charcoalized. To the filtrate, acetone (720 mL) was added over 1-2 h and filtered to get ceftriaxone sodium. The wet material of ceftriaxone sodium thus obtained was dissolved in water (120 mL) followed by addition of acetone (222 mL). The solution was cooled to −5 to −15° C. and the impurity separated as a sticky mass. The clear solution was separated and the temp raised to 18-22 C. Acetone (624 mL) was added under stirring over 1 h, filtered and washed with acetone. Drying under vacuum afforded pure ceftriaxone sodium.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07339055B2
출처 데이터셋uspto-grants-2008_03
ORD IDord-45ff88a5c13b44a99d551d3ded592b2d
출처 메모uspto-grants-2008_03