HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Diethylamino)sulfur trifluoride → 8-chloro-5-(4-chlorophenyl)-5-fluoro-5H-indeno[1,2-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 8-chloro-5-(4-chlorophenyl)-5H-indeno[1,2-d]pyrimidin-5-ol | HCID 14257087 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 8-chloro-5-(4-chlorophenyl)-5-fluoro-5H-indeno[1,2-d]pyrimidine | HCID 14257097 | 75.9% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A mixture of 3.0 g of 8-chloro-5-(4-chlorophenyl)-5H-indeno[1,2-d]pyrimidin-5-ol in 50 ml of methylene chloride was cooled to 0° C. under a nitrogen atmosphere. Approximately 2.7 g of diethylaminosulfur trifluoride were added and the reaction was stirred overnight. The mixture was poured into an iced solution of potassium bicarbonate and extracted with ethyl acetate. The organic extract was washed with a sodium bicarbonate solution and a sodium chloride solution, dried over magnesium sulfate, and concentrated in vacuo. Crystallization from ethyl acetate/isooctane provided 2.29 g of the desired title product, m.p. 236°-237° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04769378 |
| Source dataset | uspto-grants-1988_09 |
| ORD ID | ord-ea165d1e36bf40e283f87d7dc47a953e |
| Source note | uspto-grants-1988_09 |