HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → 2-{7-[(3,4-Difluorophenyl)methoxy]-1,5-naphthyridin-3-yl}acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (7-((3,4-Difluorobenzyl)oxy)-1,5-naphthyridin-3-yl)methanol | HCID 86301659 | — |
| Reactant | (7-((3,4-Difluorobenzyl)oxy)-1,5-naphthyridin-3-yl)methyl methanesulfonate | HCID 90418375 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-{7-[(3,4-Difluorophenyl)methoxy]-1,5-naphthyridin-3-yl}acetonitrile | HCID 86301660 | 64% |
Reaction Steps
(7-((3,4-difluorobenzyl)oxy)-1,5-naphthyridin-3-yl)methyl methanesulfonate. To a solution of (7-((3,4-difluorobenzyl)oxy)-1,5-naphthyridin-3-yl)methanol (Example 73, 90 mg, 0.3 mmol) in DCM (4 mL) was added methanesulfonyl chloride (0.05 mL, 0.61 mmol) followed by TEA (0.06 mL, 0.43 mmol). The reaction mixture was stirred at RT for 1 h and quenched with saturated NaHCO3 solution. The mixture was extracted with DCM (2×) and the combined organic layers were dried, filtered and concentrated under reduced pressure. Purification (FCC, SiO2, 0-80%, EtOAc/hexanes) afforded the title compound as a white solid (73 mg, 64%). [M+H]=381.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09150572B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-8d7cd42cd04b41eb8847ef2ddfc9f335 |
| Source note | uspto-grants-2015_10 |