HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → 4-Benzylamino-6-chloropyridine-3-carboxyamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4,6-Dichloropyridine-3-carboxyamide | HCID 131730931 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Benzylamino-6-chloropyridine-3-carboxyamide | HCID 131730930 | 88.6% |
Reaction Steps
5.00 g of 4,6-dichloropyridine-3-carboxyamide synthesized according to the method described in US 2006/0217417 was dissolved in 50 mL of ethanol, to which 3.37 g of benzylamine and 4.40 g of N,N-diisopropylethylamine were added, and heated at reflux for 12 hours. After cooling, the solvent was evaporated, and 100 mL of water was added to the residue. After cooling with ice, the deposited crystals were filtered, washed with water and hexane, and air-dried. It was further dried under reduced pressure (100° C., 2 hours) to obtain the title compound (5.96 g, 87%) as light yellow needle crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08575153B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-3bd9051c88f447a89e495a4a8183fa6f |
| Source note | uspto-grants-2013_11 |