Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N,N-Diethyl-p-phenylenediamine | HCID 7120 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Reactant | HCID 90370210 | HCID 90370210 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 90370305 | HCID 90370305 | — |
Reaction Steps
A mixture of 150 mg of 4-{[(2-{[3-(morpholin-4-ylmethyl)benzoyl]amino}-4,5,6,7-tetrahydro-1-benzothiophen-3-yl)carbonyl]amino}benzoic acid, 57 mg of N,N-diethyl-p-phenylenediamine, 61 mg of WSC.hydrochloride, 42 mg of HOBt, and 1.5 mL of methylene chloride was stirred for 3 hours at room temperature. Water was added to the reaction mixture, followed by extraction with methylene chloride. The organic layer was dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue was purified by basic silica gel column chromatography (2% methanol/chloroform), thereby obtaining an oily material. Methanol and 4.0 M hydrogen chloride/ethyl acetate solution were added to this material, and the solution was concentrated under reduced pressure. The residue was treated with ethyl acetate, thereby obtaining 85 mg of N-(4-{[4-(diethylamino)phenyl]carbamoyl}phenyl)-2-{[3-(morpholin-4-ylmethyl)benzoyl]amino}-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide dihydrochloride.
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-436f89e9ac8d4116af69d529234e184d |
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| Source note | uspto-grants-2015_06 |
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