HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → N-[(4-Chlorophenyl)methyl]-7-(dimethylamino)-4-hydroxy-3-quinolinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 178507324 | HCID 178507324 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[(4-Chlorophenyl)methyl]-7-(dimethylamino)-4-hydroxy-3-quinolinecarboxamide | HCID 178482605 | — |
Reaction Steps
Sodium cyanoborohydride (96 mg) is added to a mixture of 100 mg 7-amino-N-[(4-chlorophenyl)methyl]-4-hydroxy-3-quinolinecarboxamide and 91 mg paraformaldehyde in 5 mL of acetic acid. After 2 days the mixture is diluted with 5 mL of distilled water (use of more water causes the product to precipitate as an oil). The mixture is stirred an additional 10 min and then the product is collected by filtration. It is washed with three 1 mL portions of 50% aqueous acetic acid and dried in a stream of air. It is dried at 20 torr/24 h/75° C. The product is obtained as mg of an off-white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06093732 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-57c1d3e902b744e98b224443f64b98d0 |
| Source note | uspto-grants-2000_07 |