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HRID 2923생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물N-(tert-butoxycarbonyl)glycineHCID 78288—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물2,6-Dimethoxy-4-methylaniline hydrochlorideHCID 18936489—
용매Diisopropyl EtherHCID 7914—
용매TriethylamineHCID 8471—
용매Ethyl AcetateHCID 8857—
생성물N-tert-butyloxycarbonyl-[(2,6-dimethoxy-4-methylphenyl)carbamoyl]methylamineHCID 1893646596%

반응 단계

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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731340
출처 데이터셋uspto-grants-1998_03
ORD IDord-9cb77feee68640b1aefc6e6668171bff
출처 메모uspto-grants-1998_03