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HRID 37349作成日:2026年10月26日

Tributylvinyltin → Diphenylmethyl 7-Phenoxyacetamido-3-vinyl-3-cephem-4-carboxylate

https://huagongshe.com/reaction/37349

反応式

関与物質

役割名称HCID仕込み量
反応物TributylvinyltinHCID 81998—
反応物Diphenylmethyl 7-Phenoxyacetamido-3-[(fluorosulfonyl)oxy]-3-cephem-4-carboxylateHCID 88424184—
触媒palladium(II) acetateHCID 167845—
溶媒Ethyl AcetateHCID 8857—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物Diphenylmethyl 7-Phenoxyacetamido-3-vinyl-3-cephem-4-carboxylateHCID 1460893788.8%

反応手順

A solution of palladium (II) acetate (3.6 mg, 0.016 mmol, 0.1 eq.) in 1-methyl-2-pyrrolidinone (2 mL) was treated with vinyl tri-n-butylstannane (58.4 mL, 0.2 mmol, 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 mmol, 1.0 eq.) in one portion and the reaction mixture was allowed to stir for 10 minutes. The reaction mixture was diluted with ethyl acetate and washed with 3×20 mL of water. The organic fraction was dried over magnesium sulfate then concentrated. The crude brown residue was 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 (75 mL), which upon concentration furnished 74.8 mg (85%) of the title compound as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420269
出典データセットuspto-grants-1995_05
ORD IDord-d1f2a9fd35f84e6e8a411800ef17dff0
出典メモuspto-grants-1995_05