HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-bromo-N-methyl-N-(tetrahydro-furan-2-ylmethyl)-benzenesulfonamide → HCID 178482879, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-bromo-N-methyl-N-(tetrahydro-furan-2-ylmethyl)-benzenesulfonamide | HCID 61059994 | — |
| Reactant | HCID 178516005 | HCID 178516005 | — |
| Reactant | 7-(2-{6-[4-(azetidine-1-sulfonyl)-phenyl]-3H-imidazo[4,5-b]pyridin-2-yl}-ethyl)-azepan-2-one | HCID 178516007 | — |
| Product | HCID 178482879 | HCID 178482879 | — |
Reaction Steps
The title compound is synthesized as described for 7-(2-{6-[4-(azetidine-1-sulfonyl)-phenyl]-3H-imidazo[4,5-b]pyridin-2-yl}-ethyl)-azepan-2-one (compound B6) from 458 mg of 4-bromo-N-methyl-N-(tetrahydro-furan-2-ylmethyl)-benzenesulfonamide (compound C7) and 300 mg of 7-[2-(6-bromo-3H-imidazo[4,5-b]pyridin-2-yl)-ethyl]-azepan-2-one (compound C1). Purification by chromatography on flash silica gel (eluent gradient: dichloromethane/0-20 vol. % ethanol) yields 174 mg of the title compound as a waxy solid. ESI-MS: 512.4 (MH+). TLC: Rf=0.30 (dichloromethane/ethanol 10:1 parts by volume).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07790710B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-6c589fc5e96c49088af1109abc3b2758 |
| Source note | uspto-grants-2010_09 |