Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929307Generated: October 30, 2026

Diisopropylethylamine → HCID 68470489, compound

https://huagongshe.com/reaction/1929307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantTert-butoxycarbonylalanineHCID 85082—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-Amino-1-methyl-5-phenyl-1,3-dihydro-2H-azepin-2-oneHCID 57346749—
ReactantHCID 178526939HCID 178526939—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 68470489HCID 6847048997%

Reaction Conditions

Temperature10 °C

Reaction Steps

3-Amino-1-methyl-5-phenyl-1,3-dihydro-azepin-2-one (330 g, 1.54 mol) is combined with dichloromethane (3 L), N-(tert-butoxycarbonyl)-L-alanine (291.4 g, 1.54 mol), and hydroxybenzotriazole hydrate (259.5 g, 1.617 mol). The solution is cooled to about 10° C. To this solution is added diisopropylethylamine (335.4 mL, 1.925 mol) followed by 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (310.1 g, 1.617 mol) and the contents are allowed to gradually warm to room temperature. After 3.5 hours, the reaction contents are poured into water (1000 mL) and the layers are allowed to separate. The organic layer is further washed with water (1000 mL), 0.1 N HCl (1000 mL), saturated NaHCO3 solution (1000 mL) and finally saturated aqueous sodium chloride solution. The dichloromethane layer is dried over Na2SO4, filtered, and concentrated via rotary evaporation to provide the title compound (about 574 g, 97%) as a tan foam. The material is of sufficient purity to use directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188069B2
Source datasetuspto-grants-2012_05
ORD IDord-85745c656adc4f738dabd64eda702fee
Source noteuspto-grants-2012_05