Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 16660493 | HCID 16660493 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58875086 | HCID 58875086 | — |
Reaction Steps
EDCI (75 mg, 0.39 mmol) and HOBt (49 mg, 0.36 mmol) are added to a solution of 1-{3-[(R)-2-[3-(phenylsulphonylamino)-phenyl]-2-hydroxy-ethylamino]-3-methyl-butyl}-1H-indole-5-carboxylic acid-hydrotrifluoroacetate (Example 6; 100 mg, 0.16 mmol) in 2 ml DMF. Then the reaction mixture is stirred for 60 minutes at RT and combined with DIPEA (66 μl, 0.39 mmol). After 10 minutes stirring at RT a solution of dimethylamine in THF (2.0M; 2.5 ml, 5.0 mmol) is added. After 22 hours stirring at RT the solvent is eliminated in vacuo and the residue is chromatographed on Microsorb C18-reverse-phase [acetonitrile (0.1% TFA)/water (0.13% TFA)=10:90→100:0]. After freeze-drying the salt is converted into the base in ethyl acetate with semisaturated sodium hydrogen carbonate solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07754756B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-4406ffc3bf0e4eb49dd2d6c7c0ebe689 |
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| Source note | uspto-grants-2010_07 |
|---|