Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | Methyl 4-((1S)-1-aminoethyl)benzoate | HCID 17751895 | — |
| Reactant | 2-Methyl-4-(4-(trifluoromethyl)benzyl)-4H-thieno[3,2-b]pyrrole-3-carboxylic acid | HCID 67182624 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 44818729 | HCID 44818729 | 47% |
Reaction Steps
A mixture of 0.043 g of 2-methyl-4-(4-trifluoromethyl-benzyl)-4H-thieno[3,2-b]pyrrole-3-carboxylic acid, 0.060 g of (S)-4-(1-amino-ethyl)-benzoic acid methyl ester, 0.040 g of HOBT-hydrate, 0.054 g of ethyl-dimethylaminopropyl-carbodiimide hydrochloride (EDCI) and 0.060 ml of N-methylmorpholine in 2 ml of DMF was stirred at room temperature for 18 h. The reaction was then quenched with 1 ml of water and 2 ml of saturated NaHCO3 solution. The resulting mixture extracted with 15 ml of EtOAc. The organic layer was dried over Na2SO4, filtered, and concentrated to give the crude methyl ester which was dissolved in 2 ml THF, 2 mL MeOH and 0.5 mL water and treated with 0.5 mL of 1M LiOH solution. After stirring for 24 h at room temperature, the reaction mixture was concentrated under reduced pressure to remove THF and MeOH. The residue was diluted with 2 mL of water and treated with 0.3 mL of AcOH with vigorous stirring. After stirring for 2 h, the solid was collected by filtration and air-dried to give 0.029 g of the title compound as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08404736B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-d4a17d1c805a4cbfa9afabf65f2dc547 |
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| Source note | uspto-grants-2013_03 |
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