Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873775Generated: October 27, 2026

Diisopropylethylamine → tert-butyl N-[N-[2-(2,6-dimethylphenoxy)acetyl]carbamimidoyl]carbamate

https://huagongshe.com/reaction/873775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(2,6-Dimethylphenoxy)acetic acidHCID 101369—
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-[2-(2,6-dimethylphenoxy)acetyl]carbamimidoyl]carbamateHCID 14943409694%

Reaction Steps

(2,6-Dimethylphenoxy)acetic acid (5.41 g; 30 mmol), diisopropylethylamine (19.39 g; 150 mmol), tert-butyl amino(imino)methylcarbamate (5.73 g; 36 mmol), and 1-hydroxybenzotriazole monohydrate (5.52 g; 36 mmol) were dissolved in N,N-dimethylformamide (120 mL), 2-(1H)-benzotriazol-1-yl-1,1,3,3-tetramethyluronium hexafluorophosphate (13.66 g; 36 mmol) was added thereto, and the mixture was stirred for 65 hours at room temperature. To the reaction solution, ethyl acetate (400 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 crystals were dispersed in diethyl ether, collected by filtration and dried to give 9.03 g of the title compound (yield 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975411B2
Source datasetuspto-grants-2015_03
ORD IDord-320524c1c0524f128ac0d46c9b25fbe3
Source noteuspto-grants-2015_03