HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 6-Chloro-2-(ethylamino)pyridine-3-carbonyl fluoride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Cyanuric fluoride | HCID 12664 | — |
| Reactant | 6-Chloro-2-(ethylamino)nicotinic acid | HCID 63376479 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Chloro-2-(ethylamino)pyridine-3-carbonyl fluoride | HCID 86714574 | 99% |
Reaction Steps
To a suspension of 10.5 g (52.3 mmol) of the compound obtained in step 1.1 in dichloromethane (250 ml) are successively added 4.2 ml (52.3 mmol) of pyridine and 8.4 ml (99.6 mmol) of cyanuric fluoride. The mixture is stirred for 3 hours at room temperature and then filtered. The solid is rinsed with dichloromethane (100 ml) and the filtrate is washed twice with ice-cold water (60 ml). The organic phase is dried over Na2SO4 and then concentrated under reduced pressure. 10.44 g of product are obtained, the form of an orange-coloured oil. Yield=99%. The product is used without purification in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436011B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-3e6fcac51b144091a84abeee34028be9 |
| Source note | uspto-grants-2013_05 |