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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007690Generated: October 28, 2026

Diisopropylethylamine → (S)-2-{[1-(1-Cyclohexyl-2-furan-3-yl-1H-benzoimidazol-5-yl)-methanoyl]-amino}-3-(4-nitrophenyl)-propionic Acid Methyl Ester

https://huagongshe.com/reaction/1007690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Cyclohexyl-2-(furan-3-yl)-1H-benzimidazole-5-carboxylic acidHCID 491113—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantMethyl 4-nitro-L-phenylalaninate hydrochlorideHCID 11715866—
SolventAcetic AcidHCID 176—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product(S)-2-{[1-(1-Cyclohexyl-2-furan-3-yl-1H-benzoimidazol-5-yl)-methanoyl]-amino}-3-(4-nitrophenyl)-propionic Acid Methyl EsterHCID 6931443092%

Reaction Steps

The carboxylic acid of example 2 (0.500 g, 1.61 mmol), TBTU (0.621 g, 1.94 mmol) and 4-nitro-L-phenylalanine methyl ester hydrochloride (0.461 g, 1.77 mmol) were dissolved in DMSO (2.0 mL) and DIEA (6.44 mmol, 1.12 mL) was added. The mixture was stirred for 2 h at room temperature (HPLC: complete). The reaction mixture was added dropwise with stirring to a mixture of water (45 mL) and AcOH (0.8 mL). The precipitate that formed was collected by filtration, washed with water and dried (0.768 g, 92% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794404B2
Source datasetuspto-grants-2004_09
ORD IDord-45760c7c2a8c445a84c8af3cba7fc9b6
Source noteuspto-grants-2004_09