HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731645Generated: October 25, 2026
Cyclopropanecarboxylic acid → Cyclopropanecarboxylic acid [2-(5-methyl-3-phenyl-isoxazol-4-yl)-imidazo[1,2-a]pyridin-7-yl]-amide
https://huagongshe.com/reaction/731645
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropanecarboxylic acid | HCID 15655 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium chloride dihydrate | HCID 23713072 | — |
| Reactant | 2-(5-Methyl-3-phenyl-isoxazol-4-yl)-imidazo[1,2-a]pyridin-7-ylamine | HCID 24738830 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Cyclopropanecarboxylic acid [2-(5-methyl-3-phenyl-isoxazol-4-yl)-imidazo[1,2-a]pyridin-7-yl]-amide | HCID 24738831 | 12% |
Reaction Steps
A solution of 2-(5-methyl-3-phenyl-isoxazol-4-yl)-imidazo[1,2-a]pyridin-7-ylamine (92 mg, 0.32 mmol) in DMF (0.2 mL) was added to a solution containing cyclopropanecarboxylic acid (24.8 mg, 0.29 mmol), N,N,N′,N′-tetramethyl-O-(benzotriazol-1-yl)uranium tetrafluoroborate (101.7 mg, 0.32 mmol), N,N-diisopropyl ethyl amine (247 μL, 1.44 mmol) in DMF (0.3 mL) and the resulting mixture stirred at room temperature overnight and then heated at 110° C. for 2.5 h. The resulting mixture was then poured into a mixture of brine: water (1:1) and extracted with ethyl acetate. The combined organic layers were then washed with brine, dried over sodium sulphate and evaporated to leave a brown solid. Purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 0:100) afforded the title compound (12.4 mg, 12%) which was obtained as an off-white solid. MS: m/e 359.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07585874B2 |
|---|
| Source dataset | uspto-grants-2009_09 |
|---|
| ORD ID | ord-71e6d567bfd9432c81432372000248ed |
|---|
| Source note | uspto-grants-2009_09 |
|---|