HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889619Generated: October 27, 2026
Triethylamine → N-(Biphenyl-4-ylmethyl)-3,5-dichloro-N-(3-((4-cyanophenylsulfonamido)methyl)benzyl)-2-hydroxybenzenesulfonamide
https://huagongshe.com/reaction/1889619
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Cyanobenzenesulfonyl chloride | HCID 39497 | — |
| Reactant | N-(3-(Aminomethyl)benzyl)-N-(biphenyl-4-ylmethyl)-3,5-dichloro-2-hydroxybenzenesulfonamide | HCID 58531388 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(Biphenyl-4-ylmethyl)-3,5-dichloro-N-(3-((4-cyanophenylsulfonamido)methyl)benzyl)-2-hydroxybenzenesulfonamide | HCID 66634086 | 60.2% |
Reaction Steps
To a solution of 4-cyanobenzene-1-sulfonyl chloride (26 mg, 0.13 mmol) in CH2Cl2 (3 ml) was added Et3N (0.07 ml, 0.49 mmol) followed by N-(3-(aminomethyl)benzyl)-N-(biphenyl-4-ylmethyl)-3,5-dichloro-2-hydroxybenzenesulfonamide (65 mg, 0.12 mmol) at rt under nitrogen. The reaction mixture was stirred at 25° C. for 2 h. It was concentrated and the residue was purified by preparative HPLC. Fractions containing the desired product were combined, concentrated, and lyophilized to give the product as a white solid (50 mg, 56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08501992B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-e038c49ad2014672ae85f97496557b92 |
|---|
| Source note | uspto-grants-2013_08 |
|---|