HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 66616453, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3,5-Dichloro-2-hydroxybenzenesulphonyl chloride | HCID 90078 | — |
| Reactant | HCID 58531526 | HCID 58531526 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66616453 | HCID 66616453 | 51.6% |
Reaction Steps
To a solution of N-((5-(aminomethyl)-4′-fluorobiphenyl-3-yl)methyl)-N-(4-fluorobenzyl)-4-methylbenzenesulfonamide (40 mg, 0.081 mmol) and Et3N (40 mg, 0.395 mmol) in CH2Cl2 (4 mL) at rt was added solid 3,5-dichloro-2-hydroxybenzene-1-sulfonyl chloride (21.24 mg, 0.081 mmol) with stirring. The reaction was complete within an hour. The mixture was concentrated and the residue was purified by prep HPLC to provide the desired product as a white solid (30 mg). 1H NMR (CDCl3): δ 7.72 (d, J=8.2 Hz, 2H), 7.51 (d, J=2.2 Hz, 1H), 7.34-6.83 (m, 14H), 5.32 (t, J=6.0 Hz, 1H), 4.25 (s, 2H), 4.245 (s, 2H), 4.12 (d, J=6.0 Hz, 2H), 2.43 (s, 3H); MS (ESI): (M+H)+=717.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08501992B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-8725b57357b840429fad46686453bda5 |
| Source note | uspto-grants-2013_08 |