HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 25255787, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | 5-Fluoro-2-(methylsulfonyl)benzoic acid | HCID 2782735 | — |
| Reactant | HCID 59447445 | HCID 59447445 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 25255787 | HCID 25255787 | — |
Reaction Steps
To a 10 ml vial was added 5-fluoro-2-(methylsulfonyl)benzoic acid (35.5 mg, 0.163 mmol), 3-(1-methyl-1-{[3-(trifluoromethyl)phenyl]sulfonyl}ethyl)azetidine (50 mg, 0.163 mmol), Bop reagent (79 mg, 0.179 mmol), diisopropylethyl amine (0.142 ml, 0.813 mmol) and 1 ml dimethylformamide. The resulting solution was stirred at room temperature for 1 hour. It was diluted with 1 m dimethyl sulfoxide, 0.5 ml water and 0.1 ml trifluoroacetic acid. This mixture was loaded on to reverse phase column directly eluted with water acetonitrile gradient solvent to give the title compound as a fluffy white solid after lyophilizing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08304434B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-76f8fb7cc58e4a31bf16d136a227ebca |
| Source note | uspto-grants-2012_11 |