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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873781Generated: October 31, 2026

Diisopropylethylamine → tert-butyl N-[N-[3-(2,4,6-trimethylphenyl)propanoyl]carbamimidoyl]carbamate

https://huagongshe.com/reaction/873781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(2,4,6-Trimethylphenyl)propanoic acidHCID 232536—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantTert-butyl amino(imino)methylcarbamateHCID 86691067—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Producttert-butyl N-[N-[3-(2,4,6-trimethylphenyl)propanoyl]carbamimidoyl]carbamateHCID 14943410493%

Reaction Steps

3-Mesitylpropionic acid (4.40 g; 23 mmol), diisopropylethylamine (14.8 g; 115 mmol), tert-butyl amino(imino)methylcarbamate (4.40 g; 28 mmol), and 1-hydroxybenzotriazole monohydrate (4.22 g; 28 mmol) were dissolved in N,N-dimethylformamide (92 mL), 2-(1H)-benzotriazol-1-yl-1,1,3,3-tetramethyluronium hexafluorophosphate (10.5 g; 28 mmol) was added thereto, and the mixture was stirred for 17 hours at room temperature. To the reaction solution, ethyl acetate (300 mL) was added, and the mixture was washed with 10% aqueous citric acid solution, brine, saturated aqueous sodium bicarbonate solution, and then brine. The organic layer was dried over anhydrous magnesium sulfate and then distilled under reduced pressure. The resulting oily substance was crystallized from diethyl ether/diisopropyl ether, collected by filtration and dried to give 7.10 g of the title compound (yield 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975411B2
Source datasetuspto-grants-2015_03
ORD IDord-7d97125c53b141c69e8201dc366f5e1c
Source noteuspto-grants-2015_03