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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733326Generated: October 31, 2026

Diisopropylethylamine → HCID 59979241, compound

https://huagongshe.com/reaction/733326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant(2R)-2-Aminopropanamide hydrochlorideHCID 2775814—
ReactantHCID 59979225HCID 59979225—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 59979241HCID 5997924162.2%

Reaction Steps

(S)-2-[(R)-5-(4-Cyano-benzyl)-7-(3,5-dichloro-phenyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-sulfonylamino]-propionic acid (see Example 14) (0.05 g, 0.091 mmol) was dissolved in anhydrous DMF (2 mL) and TBTU (0.044 g, 0.137 mmol) was added to the reaction solution. The reaction mixture was stirred at room temperature for 10 min and D-alaninamide hydrochloride (0.017 g, 0.137 mmol) was added to the mixture followed by N,N-diisopropylethylamine (0.039 mL, 0.227 mmol). The reaction mixture was stirred at room temperature for another 15 min. The mixture was then diluted with EtOAc (10 mL) and washed with water, 1 N HCl, saturated NaHCO3 and then water. The organic phase was dried over Na2SO4 and concentrated. The crude product was purified by silica gel preparative thin layer chromatography to afford 0.035 g of the title compound as a white foam (M+1, 618.2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589115B2
Source datasetuspto-grants-2009_09
ORD IDord-64c21f6a019e4229ba5fad0815e36e47
Source noteuspto-grants-2009_09