HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513805Generated: October 31, 2026
Ammonium formate → 2-amino-N-(4-methoxy-quinolin-8-yl)benzenesulfonamide
https://huagongshe.com/reaction/513805
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 2-Amino-N-(7-chloro-4-methoxy-quinolin-8-yl)-benzenesulfonamide | HCID 68183053 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-amino-N-(4-methoxy-quinolin-8-yl)benzenesulfonamide | HCID 68182990 | 32.2% |
Reaction Steps
10% Pd—C (97 mg) was added to a solution of 2-amino-N-(7-chloro-4-methoxy-quinolin-8-yl)-benzenesulfonamide 570 (470 mg, 1.8 mmol), ammonium formate (571 mg, 9.2 mmol) in 50% AcOH (10 ml) and the mixture was heated to 70° C. for 15 h. After cooling, the solvent was removed in vacuo. The residue was dissolved in EtOAc (100 ml) and the organic phase was washed with sat. NaHCO3 solution (50 ml), dried (MgSO4) concentrated in vacuo. The crude residue was purified by column chromatography DCM/MeOH (99:1) as the eluent to give the title compound (191 mg, 32%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09102688B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-a01f488307ec41a694405a51936e1d49 |
|---|
| Source note | uspto-grants-2015_08 |
|---|