HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2-(Aminoethyl)-6-chloronicotinic acid fluoride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2,4,6-Trifluoro-1,2,3-triazine | HCID 21694433 | — |
| Reactant | 2-(Aminoethyl)-6-chloronicotinic acid | HCID 86642333 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Aminoethyl)-6-chloronicotinic acid fluoride | HCID 87400373 | 99.7% |
Reaction Steps
2 ml (24.8 mmol) of pyridine and 4.2 ml (49.8 mmol) of 2,4,6-trifluorotriazine are added to a suspension of 5.0 g (24.8 mmol) of 2-(aminoethyl)-6-chloronicotinic acid in 125 ml of dichloromethane. The mixture is stirred for 3 hours at ambient temperature and then filtered. The solid is rinsed with 50 ml of dichloromethane and the filtrate is washed twice with 60 ml of ice-cold water. The organic phase is dried over Na2SO4 and the solvent is evaporated off under reduced pressure. 5.01 g of product are obtained in the form of an orange oil. Yield=99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08470847B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-e0b571ab32624b038919e26a9dcf91a4 |
| Source note | uspto-grants-2013_06 |