HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfanilamide → HCID 25132458, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfanilamide | HCID 5333 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | HCID 57635191 | HCID 57635191 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 25132458 | HCID 25132458 | — |
Reaction Steps
The carboxylic acid intermediate 18D (400 mg) and DIEA (600 μL) were dissolved in DMF (10 mL). An aliquot of this stock solution (400 μL) was dispensed into a vial charged with 4-aminobenzene-sulfonamide (0.10 mmol). TBTU was added (0.50 mmol) to the vial and the mixture was stirred at room temperature for 2 hours. The crude mixture was purified by prep LC-MS using a gradient elution of 5% to 95% MeCN/water in 15 min. The product was taken up with DCM and diluted with hexanes. Evaporation under nitrogen flow gave the desired product, Compound 208 as a solid. LCMS (+ESI) m/z 464 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859538B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-374943debe0c4a1fa9b1242a01d65bed |
| Source note | uspto-grants-2014_10 |