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HRID 362590作成日:2026年10月27日

Triethylamine → Cefotaxime

https://huagongshe.com/reaction/362590

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物TriphenylphosphineHCID 11776—
反応物7-Aminocephalosporanic acidHCID 441328—
反応物(alphaZ)-2-Amino-alpha-(methoxyimino)-4-thiazoleacetic acidHCID 5486924—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒DimethylacetamideHCID 31374—
生成物CefotaximeHCID 5742673—

反応手順

2,2'-Dithio-bis-5-methyl-1,3,4-thiadiazole (48.09 g) and (Z)-2-(2-aminothiazol-4-yl)-2-methoxyiminoacetic acid (23.38 g) were suspended in tetrahydrofuran (297 ml) and triphenylphosphine (48.09) was added at 20°-25° C. This mixture was stirred for half an hour to generate 2-mercapto-5-methyl-1,3,4-thiadiazolyl-(Z)-2-(2-aminothiazol-4-yl)-2-methoxyimino acetate in solution. Thereafter, the reaction mixture was cooled to 3°-5° C., diluted with N,N-dimethylacetamide (46.8 ml), water (297 ml) and 7-aminocephalosporanic acid (27.2 g) was added, followed by triethylamine addition in 20 min. The reaction was continued for 3-4 hours at 3°-5° C. Thereafter, acetic acid (18 g) and water (100 ml) were added and the aqueous layer was thoroughly extracted with methylene chloride to remove tetrahydrofuran and other by-products. The aqueous phase containing triethylamine salt of cefotaxime acid was mixed with excess isopropyl alcohol (250 ml) and acidified to pH 2.80 at 0°-5°° C. with hydrochloric acid to precipitate cefotaxime acid. The mixture was then filtered, the solids washed with water, isopropyl alcohol and dried to obtain cefotaxime acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05869649
出典データセットuspto-grants-1999_02
ORD IDord-6b1ea39a5b6c4a2999cf84051403682a
出典メモuspto-grants-1999_02