HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexylamine → 6-Chloro-N4-hexyl-2,4-pyrimidinediamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexylamine | HCID 8102 | — |
| Reactant | 2-Amino-4,6-dichloropyrimidine | HCID 65522 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Chloro-N4-hexyl-2,4-pyrimidinediamine | HCID 11183788 | 62% |
Reaction Steps
50 g of 2-amino-4,6-dichloropyrimidine were suspended in 350 ml of absolute ethanol in a reactor. 181.5 ml of hexylamine (reagent A) were added in a single portion and the mixture was refluxed for 3 h. The medium was evaporated under vacuum. The oil obtained was taken up in 600 ml of water with stirring for 1 h, 30 min. The precipitate was filtered off, washed and dried in a heated desiccator. 43.5 g of the expected compound were thus obtained, for a yield of 62%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06511659B2 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-29e605362eb04f1fbc3b6fc3aa351752 |
| Source note | uspto-grants-2003_01 |