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HRID 1106182作成日:2026年10月25日

Triethylamine → 6-[4-(N-Acetyl-DL-prolylamino)phenyl]-1,2-dihydro-2-oxonicotinic acid

https://huagongshe.com/reaction/1106182

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Isobutyl chloroformateHCID 62365—
反応物DL-AcetylprolineHCID 322640—
反応物6-(4-Aminophenyl)-1,2-dihydro-2-oxonicotinic acidHCID 12918956—
溶媒DichloromethaneHCID 6344—
溶媒DimethylacetamideHCID 31374—
生成物6-[4-(N-Acetyl-DL-prolylamino)phenyl]-1,2-dihydro-2-oxonicotinic acidHCID 1291896371.5%

反応条件

温度-10 °C

反応手順

To a solution of 11.8 g (75 m mol) of N-Acetyl-DL-proline and 10.5 ml (75 m mol) of triethylamine in 150 ml dichloromethane at -15° C., is added 9.75 ml (75 m mol) of isobutyl chloroformate. The reaction mixture is stirred at about -10° C. for 30 min. To this reaction mixture is added a cold solution of 11.5 g (50 m mol) of 6-(4-aminophenyl)-1,2-dihydro-2-oxonicotinic acid and 7.7 ml (55 m mol) triethylamine in 200 ml of N,N-dimethylacetamide, which is stirred while cooling in an ice bath for 3 hrs, then overnight at room temperature. The reaction mixture is evaporated to dryness, the residue is triturated with water, and the solid collected by filtration. The solid is washed with water and acetonitrile and dried to yield 13.2 g of 6-[4-(N-Acetyl-DL-prolylamino)phenyl]-1,2-dihydro-2-oxonicotinic acid, m.p. 279°-281° dec.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04311698
出典データセットuspto-grants-1982_01
ORD IDord-e8d1097d78cb4ff6a60d1ed2fb1c6646
出典メモuspto-grants-1982_01