Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984546Generated: November 1, 2026

Diisopropylethylamine → HCID 57713976, compound

https://huagongshe.com/reaction/1984546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant(7S)-7-Amino-5,7-dihydro-6H-dibenzo[b,d]azepin-6-oneHCID 25067537—
ReactantHCID 87260088HCID 87260088—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57713976HCID 5771397668%

Reaction Steps

A solution of 250 mg (1.12 mmol) (S)-7-amino-5H,7H-dibenzo[b,d]azepin-6-one and 256 mg (1.12 mmol) (RS)-2-hydroxy-2-(2,2,2-trifluoro-ethylcarbamoyl)-butyric acid in 24 ml tetrahydrofuran were cooled to 0° C. and 174 mg (0.94 mmol) 1-hydroxy-benzotriazole hydrate, 390 μl (2.23 mmol) diisopropylethylamine and 218 mg (1.12 mmol) N-(3-dimethylaminopropyl)-N′-ethyl-carbodiimide hydrochloride were added. Stirring was continued overnight at room temperature. Removal of the solvent by distillation and chromatography on silicagel with ethylacetate/heptane 2/8 yielded 330 mg (68%) (R/S)-2-ethyl-2-hydroxy-N-((S)-6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl)-N′-(2,2,2-trifluoro-ethyl)-malonamide as a colorless oil, MS (m/e): 436.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544679B2
Source datasetuspto-grants-2009_06
ORD IDord-0b2a237134b44d51a447a88f754ac693
Source noteuspto-grants-2009_06