HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl]methanesulphonamide → HCID 131716665, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl]methanesulphonamide | HCID 9837752 | — |
| Reactant | HCID 22161755 | HCID 22161755 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131716665 | HCID 131716665 | 31.1% |
Reaction Steps
A mixture of 2-[4-[(6-bromohexyl)oxy]butyl]quinoline (900 mg), N-[5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl]methanesulphonamide (800 mg) and DEA (0.52 ml) in DMF (50 ml) was heated at 100° for 4 h, cooled, and the solvent evaporated in vacuo. The residue was purified by FCC eluting with System A (39:10:1) and (34:15:1). A solution of the resulting product in methanol (10 ml) was treated with benzoic acid (61.3 mg), the solution evaporated in vacuo and triturated with dry ether (×2) to afford the title compound as a fawn powder (250 mg) m.p. 155°-157°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04963564 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-6bf5cd1989ec4f958ee870bbc5b5e568 |
| Source note | uspto-grants-1990_10 |