Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223302Generated: October 25, 2026

Diisopropylethylamine → 2-methyl-N-(5-methyl-6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl)-malonamic acid tert-butyl ester

https://huagongshe.com/reaction/2223302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant7-Amino-5-methyl-5H-dibenzo[b,d]azepin-6(7H)-oneHCID 10198626—
Reactant3-(Tert-butoxy)-2-methyl-3-oxopropanoic acidHCID 17851702—
ReactantHCID 178418300HCID 178418300—
SolventTetrahydrofuranHCID 8028—
Product2-methyl-N-(5-methyl-6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl)-malonamic acid tert-butyl esterHCID 69039766—

Reaction Steps

To a cooled solution (0° C.) of 2-methyl-malonic acid mono-tert-butyl ester (1.01 g, 5.79 mmol) and 7-amino-5-methyl-5H,7H-dibenzo[b,d]azepin-6-one (1.15 g, 4.83 mmol) in THF (8 ml) was added hydroxybenzotriazole (652 mg, 4.83 mmol), diisopropylethylamine (624 mg, 4.83 mmol)and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (925 mg, 4.83 mmol), and the mixture was stirred overnight at r.t. The solvent was evaporated, the residue was taken up in ethyl acetate, washed with water, and dried (Na2SO4). After evaporation of the solvent, the title compound, MS: m/e=395.3 (M+H+), (920 mg, 48%) was obtained by chromatographic purification of the residue (silica gel, MeOH, CH2Cl2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375099B2
Source datasetuspto-grants-2008_05
ORD IDord-2a2568255a924934a7d158f5823a28b0
Source noteuspto-grants-2008_05