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HRID 1680128作成日:2026年10月27日

4-(Dimethylamino)Benzaldehyde → 2,2-Dimethyl-3alpha-cyano-6alpha-(p-dimethylamino-alpha-hydroxybenzyl)penam

https://huagongshe.com/reaction/1680128

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Dimethylamino)BenzaldehydeHCID 7479—
反応物2,2-Dimethyl-3alpha-cyano-6alpha-bromopenamHCID 12944713—
触媒ZincHCID 23994—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物2,2-Dimethyl-3alpha-cyano-6alpha-(p-dimethylamino-alpha-hydroxybenzyl)penamHCID 70545653—
生成物2,2-Dimethyl-3alpha-cyano-6beta-(p-dimethylamino-alpha-hydroxybenzyl)penamHCID 70546902—

反応手順

A solution of 100 mg 2,2-dimethyl-3α-cyano-6α-bromopenam in 40 ml dry tetrahydrofuran is stirred with 60 mg p-dimethylaminobenzaldehyde and 500 mg zinc for about 12 hours at room temperature. The reaction mixture is then diluted in ethyl acetate, washed with aqueous sodium chloride and dried over anhydrous sodium sulfate. Chromatography of the mixture on silica gel affords, in 11:1 ratio, 2,2-dimethyl-3α-cyano-6α-(p-dimethylamino-α-hydroxybenzyl)penam and 2,2-dimethyl-3α-cyano-6β-(p-dimethylamino-α-hydroxybenzyl)penam. The 6α-compound has the following formula: ##STR39## Utilizing 7α-bromo-4-cyano-3-cephem in the above procedure similarly affords 7α-(p-dimethylamino-α-hydroxybenzyl)-4-cyano-3-cephem.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04272439
出典データセットuspto-grants-1981_06
ORD IDord-c52bc1370f8e42859dc572b0280ac4fa
出典メモuspto-grants-1981_06