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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284723Generated: October 31, 2026

Diisopropylethylamine → HCID 90051758, compound

https://huagongshe.com/reaction/2284723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzenamine, 3-ethynyl-HCID 104682—
ReactantSodium BicarbonateHCID 516892—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant(2S)-2-(((tert-butoxy)carbonyl)(methyl)amino)propanoic acidHCID 7009590—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 90051758HCID 9005175820.7%

Reaction Steps

To N-Boc-N-methyl-L-alanine (2.03 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (3.81 g) and 1-hydroxybenzotriazole monohydrate (2.70 g), N,N-dimethylformamide (20 mL) was added at room temperature, and the mixture was stirred at the same temperature for 2 hours. To the reaction mixture, N,N-diisopropylethylamine (5.2 mL) and 3-ethynylaniline (1.17 g) were added at room temperature, and the mixture was stirred at the same temperature for 1 hour and 30 minutes. To the reaction mixture, saturated aqueous sodium hydrogencarbonate and ethyl acetate were added. The organic layer was separated, washed successively with saturated aqueous sodium hydrogencarbonate and saturated aqueous sodium chloride, and then dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent, 80 to 50% hexane in ethyl acetate) to obtain (S)-tert-butyl (1-((3-ethynylphenyl)amino)-1-oxopropan-2-yl)(methyl)carbamate (G1, 626 mg) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145415B2
Source datasetuspto-grants-2015_09
ORD IDord-c5609eeec68c4df5acdbef8257818133
Source noteuspto-grants-2015_09