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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2923Generated: October 26, 2026

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

https://huagongshe.com/reaction/2923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant2,6-Dimethoxy-4-methylaniline hydrochlorideHCID 18936489—
SolventDiisopropyl EtherHCID 7914—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductN-tert-butyloxycarbonyl-[(2,6-dimethoxy-4-methylphenyl)carbamoyl]methylamineHCID 1893646596%

Reaction Steps

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%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05731340
Source datasetuspto-grants-1998_03
ORD IDord-9cb77feee68640b1aefc6e6668171bff
Source noteuspto-grants-1998_03