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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,2-Dimethylsuccinic anhydride | HCID 87067 | — |
| Reactant | HCID 90370366 | HCID 90370366 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 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 | HCID 90370180 | 84.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062032B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-bb299870febe41728ca5dc1349edb6b0 |
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| Source note | uspto-grants-2015_06 |
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