HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromopyridine → HCID 117601099, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | HCID 117601650 | HCID 117601650 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178479889 | HCID 178479889 | — |
| Product | HCID 117601099 | HCID 117601099 | — |
Reaction Steps
Butyllithium (1.6M solution in hexanes, 24 mL, 38 mmol) was added dropwise over 20 minutes to a solution of 2-bromopyridine (3.7 mL, 38 mmol in methyl-THF (100 mL) at −78° C. The reaction mixture was stirred for 1 hour and a solution of methyl 2,3-diamino-5-(3,5-dimethylisoxazol-4-yl)benzoate (2.0 g, 7.7 mmol) in 20 mL of methyl-THF was added. The reaction mixture was warmed to room temperature, stirred for 30 minutes and quenched with water. The reaction mixture was extracted with ethyl acetate and purified by silica gel chromatography (90:9:1 ethyl acetate/methanol/ammonium hydroxide) to give (2,3-diamino-5-(3,5-dimethylisoxazol-4-yl)phenyl)di(pyridin-2-yl)methanol as an orange powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09255089B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-af6c8d34fdae4db4b700b57ce08c3851 |
| Source note | uspto-grants-2016_02 |