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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873780Generated: October 30, 2026

Diisopropylethylamine → Tert-butyl({[mesityl(methyl)amino]acetyl}amino)(imino)methylcarbamate

https://huagongshe.com/reaction/873780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant[Mesityl(methyl)amino]acetic acidHCID 82113003—
ReactantTert-butyl amino(imino)methylcarbamateHCID 86691067—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl({[mesityl(methyl)amino]acetyl}amino)(imino)methylcarbamateHCID 8669107452.2%

Reaction Steps

[Mesityl(methyl)amino]acetic acid (6.67 g; 32 mmol), diisopropylethylamine (20.68 g; 160 mmol), tert-butyl amino(imino)methylcarbamate (6.11 g; 38 mmol), and 1-hydroxybenzotriazole monohydrate (5.88 g; 38 mmol) were dissolved in N,N-dimethylformamide (150 mL), 2-(1H)-benzotriazol-1-yl-1,1,3,3-tetramethyluronium hexafluorophosphate (14.56 g; 38 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, and saturated aqueous sodium bicarbonate solution. 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 5.82 g of the title compound (yield 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975411B2
Source datasetuspto-grants-2015_03
ORD IDord-df76d8704cd34a7b8a2a3944fba0c383
Source noteuspto-grants-2015_03