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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945011Generated: November 3, 2026

Diisopropylethylamine → HCID 67208776, compound

https://huagongshe.com/reaction/1945011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Carboxymethyl-cyclopentanecarboxylic acid benzyl esterHCID 21690292—
Reactant1-(2-(Benzyloxy)-2-oxoethyl)cyclopentanecarboxylic acidHCID 59608226—
ReactantHCID 67208761HCID 67208761—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67208776HCID 67208776—

Reaction Steps

Next, to a solution of EDCl (51.2 mg, 0.267 mmol), 1-hydroxy-7-azabenzotriazole (36.4 mg, 0.267 mmol) and 6:1 mixture of 1-(2-(benzyloxy)-2-oxoethyl)cyclopentanecarboxylic acid and 2-(1-(benzyloxycarbonyl)cyclopentyl)acetic acid (65.6 mg, 0.214 mmol) in DMF (1 ml), which is stirred for 1.5 hours in advance, the crude 3-amino-4-biphenyl-4-yl-butyric acid tert-butyl ester hydrochloride and DIPEA (0.093 ml, 0.535 mmol) are added. After stirring for 2.5 hours, the reaction mixture is diluted with H2O, and the products are extracted with EtOAc. The organic layer is washed with brine, dried over Na2SO4, filtered, and concentrated. The obtained residue is purified by silica gel flash column chromatography (heptane/EtOAc=100:0 to 0:100) to give crude tert-butyl 3-(1-(2-(benzyloxy)-2-oxoethyl)cyclopentanecarboxamido)-4-(biphenyl-4-yl)butanoate (38 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394853B2
Source datasetuspto-grants-2013_03
ORD IDord-a019182c99034d2ca6b81e0bcca01d25
Source noteuspto-grants-2013_03