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HRID 5546作成日:2026年10月23日

(Z)-Tri-n-butyl(1-propenyl)tin → Diphenylmethyl 7-Phenoxyacetamido-3-(Z-1-propenyl)-3-cephem-4carboxylate

https://huagongshe.com/ja/reaction/5546

反応式

関与物質

役割名称HCID仕込み量
反応物(Z)-Tri-n-butyl(1-propenyl)tinHCID 10914524—
反応物Diphenylmethyl 7-Phenoxyacetamido-3-[(fluorosulfonyl)oxy]-3-cephem-4-carboxylateHCID 88424184—
触媒palladium(II) acetateHCID 167845—
溶媒DichloromethaneHCID 6344—
生成物Diphenylmethyl 7-Phenoxyacetamido-3-(Z-1-propenyl)-3-cephem-4carboxylateHCID 1460894092.9%

反応手順

A solution of palladium (II) acetate (3.6 mg, 0.016 mmole, 0.1 eq.) in dichloromethane (2 mL) was treated with Z-1-propenyl tri-n-butylstannane (66.2 mg, 0.2 mmole, 1.2 eq.) under an inert atmosphere and allowed to stir for 3 minutes. The resulting dark suspension was then treated with diphenylmethyl 7-phenoxyacetamido-3-[(fluorosulfonyl) oxy]-3-cephem-4-carboxylate (100.0 mg, 0.16 mmole, 1.0 eq.) in one portion and the reaction mixture was allowed to stir for 10 minutes. The reaction mixture was diluted with additional dichloromethane and washed with water (1×10 mL). The organic fraction was dried over magnesium sulfate and purified by flash filtration through a pad of silica gel (W. R. Grace, 951W) first with dichloromethane (50 mL) to remove the residual stannane and then with 10% ethyl acetate in dichloromethane (50 mL) which upon concentration furnished 80.4 mg (89%) of the title compound as a pale yellow solid. The product was then recrystallized from isopropyl alcohol to afford 62.3 mg (69%) of a white solid, mp. 103°-104° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05245027
出典データセットuspto-grants-1993_09
ORD IDord-c2b21fff05b941f38cbaf9f020481d88
出典メモuspto-grants-1993_09