HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510813Generated: October 25, 2026
Trisodium phosphate dodecahydrate → N-(2-Chloro-4-methylpyridin-3-yl)-2-(cyclopropylamino)nicotinamide
https://huagongshe.com/reaction/1510813
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trisodium phosphate dodecahydrate | HCID 61473 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | 2-Chloro-N-(2-chloro-4-methyl-3-pyridinyl)-3-pyridinecarboxamide | HCID 10423868 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | N-(2-Chloro-4-methylpyridin-3-yl)-2-(cyclopropylamino)nicotinamide | HCID 9972204 | — |
Reaction Steps
2-Chloro-N-(2-chloro-4-methyl-3-pyridinyl)-3-pyridine carboxamide (15 g), trisodium phosphate dodecahydrate (20.21 g), cyclopropylamine (12.12 g) were suspended in o-xylene (45 ml) and heated to 130-140° C. for 6-8 h in S.S. Bomb with occasional shaking. Then the reaction mass was cooled to 70-75° C., diluted with o-xylene (75 ml) and DM water (45 ml) and stirred for 10 min at 70-80° C. The aqueous layer was separated and washed the organic layer with DM water (45 ml) at 70-80° C. The organic layer was concentrated at 60-65° C. under reduced pressure. The concentrated mass was cooled to 5-10° C. and stirred for 30 min. Filtered the solid obtained and washed with chilled o-xylene (15 ml, 5-10° C.). Dried the obtained solid at 55-60° C. under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08212025B2 |
|---|
| Source dataset | uspto-grants-2012_07 |
|---|
| ORD ID | ord-04b544f771af4d07817925556a9a0f07 |
|---|
| Source note | uspto-grants-2012_07 |
|---|