HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → HCID 57433640, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Pyridine-2-carbonyl chloride | HCID 135034 | — |
| Reactant | HCID 57433639 | HCID 57433639 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57433640 | HCID 57433640 | 63.1% |
Reaction Steps
With cooling with ice, 0.33 ml of triethylamine and 210 mg of picolinic acid chloride were added to a chloroform (2 ml) solution of 144 mg of 1-(2-amino-5-{[6-(5-methyl-1,2,4-oxadiazol-3-yl)pyridin-3-yl]oxy}benzyl)pyrrolidin-2-one, and stirred at room temperature for 1 hour. Water was added to it, extracted with chloroform, the organic layer was dried, the solvent was removed, and the residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=9/1 to 2/8) to obtain 117 mg of N-{4-{[6-(5-methyl-1,2,4-oxadiazol-3-yl)pyridin-3-yl]oxy}-2-[(2-oxopyrrolidin-1-yl)methyl]phenyl}pyridine-2-carboxamide as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07932394B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-4ac9386d70234febba36c5cd37b14d70 |
| Source note | uspto-grants-2011_04 |