HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Azide → Methyl 6-azido-4-(4-bromo-2-chlorophenylamino)-5-chloronicotinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Methyl 4-(4-bromo-2-chlorophenylamino)-5,6-dichloronicotinate | HCID 11603943 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 6-azido-4-(4-bromo-2-chlorophenylamino)-5-chloronicotinate | HCID 59519382 | — |
Reaction Steps
Sodium azide (4.4 g, 68 mmol) was added to a suspension of 4-(4-bromo-2-chlorophenylamino)-5,6-dichloronicotinic acid methyl ester (26) (13.89 g, 33.8 mmol) in DMF (200 mL) and the mixture allowed to stir at room temperature overnight. The solution was diluted with water (600 mL) and the resulting white precipitate was collected by filtration and washed with water. The solids were dissolved into THF. Two volumes of diethyl ether were added and the organic solution washed with brine, dried over NaSO4, filtered, and concentrated in vacuo to the desired product (27) as a light yellow solid (12.94 g, 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538120B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-85f60a9474a742ee938e2975590010d8 |
| Source note | uspto-grants-2009_05 |