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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176010Generated: October 29, 2026

Diisopropylethylamine → 4-[(2-{[3-({3-[(4-{2-[4-(Methoxycarbonyl)phenyl]ethyl}phenyl)carbamoyl]-4,5,6,7-tetrahydro-1-benzothiophen-2-yl}carbamoyl)benzyl](pentan-3-yl)amino)ethyl)(methyl)amino]-2,2-dimethyl-4-oxobutanoic acid

https://huagongshe.com/reaction/2176010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2,2-Dimethylsuccinic anhydrideHCID 87067—
ReactantHCID 90370366HCID 90370366—
Solvent1,4-DioxaneHCID 31275—
Product4-[(2-{[3-({3-[(4-{2-[4-(Methoxycarbonyl)phenyl]ethyl}phenyl)carbamoyl]-4,5,6,7-tetrahydro-1-benzothiophen-2-yl}carbamoyl)benzyl](pentan-3-yl)amino)ethyl)(methyl)amino]-2,2-dimethyl-4-oxobutanoic acidHCID 9037018084.4%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a mixture of 200 mg of methyl 4-[2-(4-{[(2-{[3-({[2-(methylamino)ethyl](pentan-3-yl)amino}methyl)benzoyl]amino}-4,5,6,7-tetrahydro-1-benzothiophen-3-yl)carbonyl]amino}phenyl)ethyl]benzoate, 48 mg of N-ethyl-N-isopropylpropan-2-amine and 4 mL of dioxane was added 44 mg of 3,3-dimethyldihydrofuran-2,5-dione, followed by stirring overnight at 65° C. The reaction mixture was concentrated under reduced pressure, ethyl acetate and water were added to the residue, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography, thereby obtaining 200 mg of 4-[(2-{[3-({3-[(4-{2-[4-(methoxycarbonyl)phenyl]ethyl}phenyl)carbamoyl]-4,5,6,7-tetrahydro-1-benzothiophen-2-yl}carbamoyl)benzyl](pentan-3-yl)amino}ethyl)(methyl)amino]-2,2-dimethyl-4-oxobutanoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062032B2
Source datasetuspto-grants-2015_06
ORD IDord-bb299870febe41728ca5dc1349edb6b0
Source noteuspto-grants-2015_06