HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfanilamide → HCID 10471014, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfanilamide | HCID 5333 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3-(1,3-Dioxolan-2-yl)-1-(4-fluorophenyl)-1-propanone | HCID 2758696 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 10471014 | HCID 10471014 | 40.7% |
Reaction Steps
A mixture of 3-(1,3-dioxolan-2-yl)-1-(4-fluorophenyl)propan-1-one (Example 8, Step 2) (1.6 g, 7.14 mmol), sulfanilamide (1.35 g, 7.86 mmol), p-toluenesulfonic acid (120 mg) and molecular sieves (4 Å, 3 g) in toluene (250 ml) was heated to reflux for 98 hours. The reaction was cooled, filtered and concentrated. The crude brownish solid (3.2 g) was purified by chromatography (silica gel, hexane/ethyl acetate, 6/4) to give 4-[2-(4-fluorophenyl)-1H-pyrrol-1-yl]benzenesulfonamide (920 mg, 40%) as a white solid: mp (DSC) 206° C. Anal Calc'd. for C16H13N2SFO2 ·0.2 H2O: C, 60.06; H, 4.22; N, 8.76; S, 10.02. Found: C, 60.13; H, 4.21; N, 8.61; S, 10.15.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05935990 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-127514f990f04c67b2ed74ba725dcf4d |
| Source note | uspto-grants-1999_08 |