Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(Piperazin-1-yl)benzene-1-sulfonamide | HCID 901897 | — |
| Reactant | 2-Chloromethyl-imidazo(1,2-A)pyridine | HCID 957614 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15409147 | HCID 15409147 | 62.5% |
Reaction Steps
A mixture of 2-(chloromethyl)imidazo[1,2-a]pyridine (0.495 g), 4-(piperazin-1-yl) benzenesulfonamide (0.717 g), triethylamine (0.456 mL), and ethylene glycol (6 mL) is stirred at 80° C. for 1.5 h. After cooling, water is added and the resulting solid is collected and washed with water and toluene. Chromatography on silica gel using methanol/dichloromethane (6/94) yields 0.69 g of the title compound; mp 238-242° C.; IR (mineral oil) 1150, 1152, 1331, 1308, 1508 cm-1. 1H NMR (DMSOd6) δ2.61. 3.28, 3.66, 6.86, 7.02, 7.06, 7.20, 7.49, 7.61, 7.85, 8.50.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05912246 |
|---|
| Source dataset | uspto-grants-1999_06 |
|---|
| ORD ID | ord-4bdd1040c5ca4266a1b85f5afa148947 |
|---|
| Source note | uspto-grants-1999_06 |
|---|