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HRID 2923作成日:2026年10月23日

Dimethylformamide → N-tert-butyloxycarbonyl-[(2,6-dimethoxy-4-methylphenyl)carbamoyl]methylamine

https://huagongshe.com/ja/reaction/2923

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物N-(tert-butoxycarbonyl)glycineHCID 78288—
反応物Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
反応物2,6-Dimethoxy-4-methylaniline hydrochlorideHCID 18936489—
溶媒Diisopropyl EtherHCID 7914—
溶媒TriethylamineHCID 8471—
溶媒Ethyl AcetateHCID 8857—
生成物N-tert-butyloxycarbonyl-[(2,6-dimethoxy-4-methylphenyl)carbamoyl]methylamineHCID 1893646596%

反応手順

6.6 g of N-Boc-glycine and 15.6 g of BOP are successively added to 100 ml of dimethylformamide and then, at 0° C., 14 ml of triethylamine are added dropwise. The mixture is left for 20 minutes at 0° C. and 6.7 g of 2,6-dimethoxy-4-methylaniline hydrochloride are then added portionwise. The reaction mixture is left at room temperature for 15 hours. 400 ml of ethyl acetate are added to the reaction mixture and the organic phase is successively washed with 3×200 ml of water, with a 1N aqueous sodium hydroxide solution and then with water. The organic phase is dried over anhydrous sodium sulphate. Evaporation of the solvent leaves a semi-crystalline residue which is solidified in diisopropyl ether to provide N-tert-butyloxycarbonyl-[(2,6-dimethoxy-4-methylphenyl)carbamoyl]methylamine, in the form of white crystals; M.p.=146° C.; Yield: 96%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731340
出典データセットuspto-grants-1998_03
ORD IDord-9cb77feee68640b1aefc6e6668171bff
出典メモuspto-grants-1998_03