Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Bromomethylcyclopropane | HCID 81503 | — |
| Reactant | HCID 10275983 | HCID 10275983 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 9806292 | HCID 9806292 | 71.5% |
Reaction Steps
To a solution of 3-{7-(cyclopentylamino)-3-[2-(cyclopentylamino)-4-pyrimidinyl]pyrazolo[1,5-a]pyridin-2-yl}phenol (400 mg, 0.88 mmol) in acetonitrile (80 mL) was added cesium carbonate (315 mg, 0.97 mmol) and (bromomethyl)-cyclopropane (0.26 mL, 2.64 mmol). The reaction mixture was heated at reflux for 6 hours. After the reaction was cooled to room temperature, ethyl acetate was added and the organic phase was washed with water, brine and dried over magnesium sulfate. Filtration and concentration followed by purification with silica gel chromatography (3:2 hexanes/ethyl acetate) gave N-cyclopentyl-3-[2-(cyclopentylamino)-4-pyrimidinyl]-2-[3-(cyclopropylmethoxy)phenyl]pyrazolo[1,5-a]pyridin-7-amine (320 mg, 71%) as yellow solid. 1H NMR (CDCl3): δ 7.97 (d, 1H), 7.78 (d, 1H), 7.33 (m, 2H), 7.18 (m, 2H), 6.98 (m, 1H), 6.30 (d, 1H), 6.02 (m, 2H), 5.08 (d, 1), 4.35 (m, 1H), 3.99 (m, 1H), 3.80 (d, 2H), 2.014 (m, 4H), 1.83–1.55 (m, 12H), 1.22 (m, 1H), 0.61 (m, 2H), 0.35 (m, 2H). MS m/z 509 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07153855B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-6318b835d3b24dbfa4b1e83bb7adda98 |
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| Source note | uspto-grants-2006_12 |
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